共 50 条
- [1] AUTOSOMAL RECESSIVE AXONAL NEUROPATHY WITH NEUROMYOTONIA DUE TO HINT1 GENE MUTATIONJOURNAL OF THE PERIPHERAL NERVOUS SYSTEM, 2014, 19 : S14 - S15Gandioli, C.论文数: 0 引用数: 0 h-index: 0机构: Fdn IRCCS Ist Neurol C Besta, Div Neuropsichiatria Infantile, Milan, Italy Fdn IRCCS Ist Neurol C Besta, Div Neuropsichiatria Infantile, Milan, ItalyTaroni, F.论文数: 0 引用数: 0 h-index: 0机构: Fdn IRCCS Ist Neurol C Besta, SOSD Genet Malattie Neurodegenerat & Metab, Milan, Italy Fdn IRCCS Ist Neurol C Besta, Div Neuropsichiatria Infantile, Milan, ItalyMilani, M.论文数: 0 引用数: 0 h-index: 0机构: Fdn IRCCS Ist Neurol C Besta, SOSD Genet Malattie Neurodegenerat & Metab, Milan, Italy Fdn IRCCS Ist Neurol C Besta, Div Neuropsichiatria Infantile, Milan, ItalyPiscosquito, G.论文数: 0 引用数: 0 h-index: 0机构: Fdn IRCCS Ist Neurol C Besta, SOSD Clin Neuropatie Degenerat Cent & Perifer, Milan, Italy Fdn IRCCS Ist Neurol C Besta, Div Neuropsichiatria Infantile, Milan, ItalyPareyson, D.论文数: 0 引用数: 0 h-index: 0机构: Fdn IRCCS Ist Neurol C Besta, SOSD Clin Neuropatie Degenerat Cent & Perifer, Milan, Italy Fdn IRCCS Ist Neurol C Besta, Div Neuropsichiatria Infantile, Milan, ItalyMoroni, I论文数: 0 引用数: 0 h-index: 0机构: Fdn IRCCS Ist Neurol C Besta, Div Neuropsichiatria Infantile, Milan, Italy Fdn IRCCS Ist Neurol C Besta, Div Neuropsichiatria Infantile, Milan, Italy
- [2] A Novel Mutation of HINT1 Gene in an Adolescent Female with Axonal Neuropathy and NeuromyotoniaJOURNAL OF PEDIATRIC NEUROLOGY, 2021, 19 (03) : 180 - 182Kara, Bulent论文数: 0 引用数: 0 h-index: 0机构: Kocaeli Univ, Fac Med, Dept Pediat, Div Child Neurol, TR-41380 Kocaeli, Turkey Kocaeli Univ, Fac Med, Dept Pediat, Div Child Neurol, TR-41380 Kocaeli, TurkeyGul, Sedat论文数: 0 引用数: 0 h-index: 0机构: Kocaeli Univ, Dept Pediat, Fac Med, Kocaeli, Turkey Kocaeli Univ, Fac Med, Dept Pediat, Div Child Neurol, TR-41380 Kocaeli, TurkeyGunes, Ayfer Sakarya论文数: 0 引用数: 0 h-index: 0机构: Kocaeli Univ, Fac Med, Dept Pediat, Div Child Neurol, TR-41380 Kocaeli, Turkey Kocaeli Univ, Fac Med, Dept Pediat, Div Child Neurol, TR-41380 Kocaeli, TurkeyMulayim, Serap论文数: 0 引用数: 0 h-index: 0机构: Kocaeli Univ, Dept Neurol, Fac Med, Kocaeli, Turkey Kocaeli Univ, Fac Med, Dept Pediat, Div Child Neurol, TR-41380 Kocaeli, TurkeyYesil, Gozde论文数: 0 引用数: 0 h-index: 0机构: Bezmialem Vakif Univ, Dept Med Genet, Istanbul, Turkey Kocaeli Univ, Fac Med, Dept Pediat, Div Child Neurol, TR-41380 Kocaeli, Turkey
- [3] Hereditary, non HINT1 related, axonal neuropathy with neuromyotoniaNEUROLOGICAL SCIENCES, 2025,Spiliopoulos, Kanellos C.论文数: 0 引用数: 0 h-index: 0机构: Univ Patras, Sch Med, Dept Neurol, Patras, Greece Univ Patras, Sch Med, Dept Neurol, Patras, GreeceVeltsista, Dimitra论文数: 0 引用数: 0 h-index: 0机构: Univ Patras, Sch Med, Dept Neurol, Patras, Greece Univ Patras, Sch Med, Dept Neurol, Patras, GreeceVeltsou, Eirini论文数: 0 引用数: 0 h-index: 0机构: Univ Patras, Mol Genet Unit, Dept Gen Biol, Sch Med, Patras, Greece Univ Patras, Sch Med, Dept Neurol, Patras, GreeceTzimogianni, Valentini论文数: 0 引用数: 0 h-index: 0机构: Univ Patras, Mol Genet Unit, Dept Gen Biol, Sch Med, Patras, Greece Univ Patras, Sch Med, Dept Neurol, Patras, GreeceSeo, Go Hun论文数: 0 引用数: 0 h-index: 0机构: 3billion Inc, Seoul, South Korea Univ Patras, Sch Med, Dept Neurol, Patras, GreeceKim, Jihye论文数: 0 引用数: 0 h-index: 0机构: 3billion Inc, Seoul, South Korea Univ Patras, Sch Med, Dept Neurol, Patras, GreeceLygerou, Zoi论文数: 0 引用数: 0 h-index: 0机构: Univ Patras, Mol Genet Unit, Dept Gen Biol, Sch Med, Patras, Greece Univ Patras, Sch Med, Dept Neurol, Patras, Greece论文数: 引用数: h-index:机构:
- [4] A CASE OF NEUROMYOTONIA AND AXONAL MOTOR NEUROPATHY: A REPORT OF A HINT1 MUTATION IN THE UNITED STATESMUSCLE & NERVE, 2015, 52 (06) : 1110 - 1113Jerath, Nivedita U.论文数: 0 引用数: 0 h-index: 0机构: Univ Iowa, Carver Coll Med, Dept Neurol, Iowa City, IA 52246 USA Univ Iowa, Carver Coll Med, Dept Neurol, Iowa City, IA 52246 USAShy, Michael E.论文数: 0 引用数: 0 h-index: 0机构: Univ Iowa, Carver Coll Med, Dept Neurol, Iowa City, IA 52246 USA Univ Iowa, Carver Coll Med, Dept Neurol, Iowa City, IA 52246 USAGrider, Tiffany论文数: 0 引用数: 0 h-index: 0机构: Univ Iowa, Carver Coll Med, Dept Neurol, Iowa City, IA 52246 USA Univ Iowa, Carver Coll Med, Dept Neurol, Iowa City, IA 52246 USAGutmann, Ludwig论文数: 0 引用数: 0 h-index: 0机构: Univ Iowa, Carver Coll Med, Dept Neurol, Iowa City, IA 52246 USA Univ Iowa, Carver Coll Med, Dept Neurol, Iowa City, IA 52246 USA
- [5] HINT1 founder mutation causing axonal neuropathy with neuromyotonia in South America: A case reportMOLECULAR GENETICS & GENOMIC MEDICINE, 2021, 9 (10):Coelho Silva Madeiro, Bianca de Aguiar论文数: 0 引用数: 0 h-index: 0机构: Univ Pernambuco, Oswaldo Cruz Univ Hosp, Recife, PE, Brazil Univ Pernambuco, Oswaldo Cruz Univ Hosp, Recife, PE, BrazilPeeters, Kristien论文数: 0 引用数: 0 h-index: 0机构: VIB UAntwerp Ctr Mol Neurol, Antwerp, Belgium Univ Pernambuco, Oswaldo Cruz Univ Hosp, Recife, PE, BrazilSantos de Lima, Elker Lene论文数: 0 引用数: 0 h-index: 0机构: Univ Pernambuco, Oswaldo Cruz Univ Hosp, Recife, PE, Brazil Univ Pernambuco, Oswaldo Cruz Univ Hosp, Recife, PE, BrazilAmor-Barris, Silvia论文数: 0 引用数: 0 h-index: 0机构: VIB UAntwerp Ctr Mol Neurol, Antwerp, Belgium Univ Pernambuco, Oswaldo Cruz Univ Hosp, Recife, PE, BrazilDe Vriendt, Els论文数: 0 引用数: 0 h-index: 0机构: VIB UAntwerp Ctr Mol Neurol, Antwerp, Belgium Univ Pernambuco, Oswaldo Cruz Univ Hosp, Recife, PE, BrazilJordanova, Albena论文数: 0 引用数: 0 h-index: 0机构: VIB UAntwerp Ctr Mol Neurol, Antwerp, Belgium Univ Pernambuco, Oswaldo Cruz Univ Hosp, Recife, PE, BrazilCartaxo Muniz, Maria Tereza论文数: 0 引用数: 0 h-index: 0机构: Univ Pernambuco, Oswaldo Cruz Univ Hosp, Recife, PE, Brazil Univ Pernambuco, Oswaldo Cruz Univ Hosp, Recife, PE, BrazilCorreia, Carolina da Cunha论文数: 0 引用数: 0 h-index: 0机构: Univ Pernambuco, Oswaldo Cruz Univ Hosp, Recife, PE, Brazil Univ Pernambuco, Oswaldo Cruz Univ Hosp, Recife, PE, Brazil
- [6] Loss-of-function mutations in HINT1 cause axonal neuropathy with neuromyotoniaNATURE GENETICS, 2012, 44 (10) : 1080 - 1083Zimon, Magdalena论文数: 0 引用数: 0 h-index: 0机构: Univ Antwerp VIB, Dept Mol Genet, Mol Neurogen Grp, B-2610 Antwerp, Belgium Univ Antwerp, Neurogenet Lab, Inst Born Bunge, B-2020 Antwerp, Belgium Univ Antwerp VIB, Dept Mol Genet, Mol Neurogen Grp, B-2610 Antwerp, BelgiumBaets, Jonathan论文数: 0 引用数: 0 h-index: 0机构: Univ Antwerp, Neurogenet Lab, Inst Born Bunge, B-2020 Antwerp, Belgium Univ Antwerp VIB, Dept Mol Genet, Neurogenet Grp, B-2020 Antwerp, Belgium Univ Antwerp Hosp, Dept Neurol, Antwerp, Belgium Univ Antwerp VIB, Dept Mol Genet, Mol Neurogen Grp, B-2610 Antwerp, BelgiumAlmeida-Souza, Leonardo论文数: 0 引用数: 0 h-index: 0机构: Univ Antwerp, Neurogenet Lab, Inst Born Bunge, B-2020 Antwerp, Belgium Univ Antwerp VIB, Dept Mol Genet, Peripheral Neuropathy Grp, B-2610 Antwerp, Belgium Univ Antwerp VIB, Dept Mol Genet, Mol Neurogen Grp, B-2610 Antwerp, BelgiumDe Vriendt, Els论文数: 0 引用数: 0 h-index: 0机构: Univ Antwerp VIB, Dept Mol Genet, Mol Neurogen Grp, B-2610 Antwerp, Belgium Univ Antwerp, Neurogenet Lab, Inst Born Bunge, B-2020 Antwerp, Belgium Univ Antwerp VIB, Dept Mol Genet, Mol Neurogen Grp, B-2610 Antwerp, BelgiumNikodinovic, Jelena论文数: 0 引用数: 0 h-index: 0机构: Univ Belgrade, Clin Neurol & Psychiat Children & Youth, Belgrade, Serbia Univ Antwerp VIB, Dept Mol Genet, Mol Neurogen Grp, B-2610 Antwerp, BelgiumParman, Yesim论文数: 0 引用数: 0 h-index: 0机构: Istanbul Univ, Dept Neurol, Istanbul Fac Med, Istanbul, Turkey Univ Antwerp VIB, Dept Mol Genet, Mol Neurogen Grp, B-2610 Antwerp, BelgiumBattaloglu, Esra论文数: 0 引用数: 0 h-index: 0机构: Bogazici Univ, Dept Mol Biol & Genet, Istanbul, Turkey Univ Antwerp VIB, Dept Mol Genet, Mol Neurogen Grp, B-2610 Antwerp, BelgiumMatur, Zeliha论文数: 0 引用数: 0 h-index: 0机构: Istanbul Univ, Dept Neurol, Istanbul Fac Med, Istanbul, Turkey Univ Antwerp VIB, Dept Mol Genet, Mol Neurogen Grp, B-2610 Antwerp, BelgiumGuergueltcheva, Velina论文数: 0 引用数: 0 h-index: 0机构: Med Univ Sofia, Dept Neurol, Sofia, Bulgaria Univ Antwerp VIB, Dept Mol Genet, Mol Neurogen Grp, B-2610 Antwerp, BelgiumTournev, Ivailo论文数: 0 引用数: 0 h-index: 0机构: Med Univ Sofia, Dept Neurol, Sofia, Bulgaria New Bulgarian Univ, Dept Cognit Sci & Psychol, Sofia, Bulgaria Univ Antwerp VIB, Dept Mol Genet, Mol Neurogen Grp, B-2610 Antwerp, BelgiumAuer-Grumbach, Michaela论文数: 0 引用数: 0 h-index: 0机构: Med Univ Graz, Dept Internal Med, Div Endocrinol & Metab, Graz, Austria Univ Antwerp VIB, Dept Mol Genet, Mol Neurogen Grp, B-2610 Antwerp, Belgium论文数: 引用数: h-index:机构:Petersen, Britt-Sabina论文数: 0 引用数: 0 h-index: 0机构: Univ Kiel, Inst Clin Mol Biol, Kiel, Germany Univ Antwerp VIB, Dept Mol Genet, Mol Neurogen Grp, B-2610 Antwerp, BelgiumMueller, Thomas论文数: 0 引用数: 0 h-index: 0机构: Innsbruck Med Univ, Dept Pediat 2, Innsbruck, Austria Univ Antwerp VIB, Dept Mol Genet, Mol Neurogen Grp, B-2610 Antwerp, BelgiumFransen, Erik论文数: 0 引用数: 0 h-index: 0机构: Univ Antwerp, Dept Mol Genet, B-2020 Antwerp, Belgium Univ Antwerp, StatUA Ctr Stat, B-2020 Antwerp, Belgium Univ Antwerp VIB, Dept Mol Genet, Mol Neurogen Grp, B-2610 Antwerp, BelgiumVan Damme, Philip论文数: 0 引用数: 0 h-index: 0机构: Univ Louvain, LIND, Louvain, Belgium VIB, Vesalius Res Ctr, Louvain, Belgium Univ Louvain, Univ Hosp Leuven, Dept Neurol, Louvain, Belgium Univ Antwerp VIB, Dept Mol Genet, Mol Neurogen Grp, B-2610 Antwerp, BelgiumLoescher, Wolfgang N.论文数: 0 引用数: 0 h-index: 0机构: Innsbruck Med Univ, Dept Neurol, Innsbruck, Austria Univ Antwerp VIB, Dept Mol Genet, Mol Neurogen Grp, B-2610 Antwerp, BelgiumBarisic, Nina论文数: 0 引用数: 0 h-index: 0机构: Univ Zagreb, Dept Paediat, Sch Med, Univ Hosp Ctr Zagreb, Zagreb 41000, Croatia Univ Antwerp VIB, Dept Mol Genet, Mol Neurogen Grp, B-2610 Antwerp, BelgiumMitrovic, Zoran论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp Ctr Zagreb, Dept Neurol, Natl Ctr Neuromuscular Dis, Zagreb, Croatia Univ Antwerp VIB, Dept Mol Genet, Mol Neurogen Grp, B-2610 Antwerp, BelgiumPrevitali, Stefano C.论文数: 0 引用数: 0 h-index: 0机构: Ist Sci San Raffaele, Inst Expt Neurol, Div Neurosci, I-20132 Milan, Italy Ist Sci San Raffaele, Dept Neurol, I-20132 Milan, Italy Univ Antwerp VIB, Dept Mol Genet, Mol Neurogen Grp, B-2610 Antwerp, BelgiumTopaloglu, Haluk论文数: 0 引用数: 0 h-index: 0机构: Hacettepe Univ, Fac Med, Dept Paediat Neurol, TR-06100 Ankara, Turkey Univ Antwerp VIB, Dept Mol Genet, Mol Neurogen Grp, B-2610 Antwerp, BelgiumBernert, Guenther论文数: 0 引用数: 0 h-index: 0机构: Gottfried von Preyersches Kinderspital, Dept Paediat, Vienna, Austria Univ Antwerp VIB, Dept Mol Genet, Mol Neurogen Grp, B-2610 Antwerp, BelgiumBeleza-Meireles, Ana论文数: 0 引用数: 0 h-index: 0机构: Univ Aveiro, Autonomous Sect Hlth Sci, P-3800 Aveiro, Portugal Coimbra Paediat Hosp, Dept Genet, Ctr Hosp, Coimbra, Portugal Univ Coimbra CHUC EPE, Coimbra, Portugal Univ Antwerp VIB, Dept Mol Genet, Mol Neurogen Grp, B-2610 Antwerp, BelgiumTodorovic, Slobodanka论文数: 0 引用数: 0 h-index: 0机构: Univ Belgrade, Clin Neurol & Psychiat Children & Youth, Belgrade, Serbia Univ Antwerp VIB, Dept Mol Genet, Mol Neurogen Grp, B-2610 Antwerp, BelgiumSavic-Pavicevic, Dusanka论文数: 0 引用数: 0 h-index: 0机构: Univ Belgrade, Fac Biol, PCR Ctr, Belgrade, Serbia Univ Antwerp VIB, Dept Mol Genet, Mol Neurogen Grp, B-2610 Antwerp, BelgiumIshpekova, Boryana论文数: 0 引用数: 0 h-index: 0机构: Med Univ Sofia, Dept Neurol, Sofia, Bulgaria New Bulgarian Univ, Dept Cognit Sci & Psychol, Sofia, Bulgaria Univ Antwerp VIB, Dept Mol Genet, Mol Neurogen Grp, B-2610 Antwerp, BelgiumLechner, Silvia论文数: 0 引用数: 0 h-index: 0机构: Innsbruck Med Univ, Div Human Genet, Innsbruck, Austria Univ Antwerp VIB, Dept Mol Genet, Mol Neurogen Grp, B-2610 Antwerp, BelgiumPeeters, Kristien论文数: 0 引用数: 0 h-index: 0机构: Univ Antwerp VIB, Dept Mol Genet, Mol Neurogen Grp, B-2610 Antwerp, Belgium Univ Antwerp, Neurogenet Lab, Inst Born Bunge, B-2020 Antwerp, Belgium Univ Antwerp VIB, Dept Mol Genet, Mol Neurogen Grp, B-2610 Antwerp, BelgiumOoms, Tinne论文数: 0 引用数: 0 h-index: 0机构: Univ Antwerp VIB, Dept Mol Genet, Mol Neurogen Grp, B-2610 Antwerp, Belgium Univ Antwerp, Neurogenet Lab, Inst Born Bunge, B-2020 Antwerp, Belgium Univ Antwerp VIB, Dept Mol Genet, Mol Neurogen Grp, B-2610 Antwerp, BelgiumHahn, Angelika F.论文数: 0 引用数: 0 h-index: 0机构: Univ Western Ontario, Dept Clin Neurol Sci, London Hlth Sci Ctr, London, ON, Canada Univ Antwerp VIB, Dept Mol Genet, Mol Neurogen Grp, B-2610 Antwerp, BelgiumZuechner, Stephan论文数: 0 引用数: 0 h-index: 0机构: Univ Miami, Miller Sch Med, Hussman Inst Human Genet, Miami, FL 33136 USA Univ Antwerp VIB, Dept Mol Genet, Mol Neurogen Grp, B-2610 Antwerp, Belgium论文数: 引用数: h-index:机构:Van Dijck, Patrick论文数: 0 引用数: 0 h-index: 0机构: Univ Louvain, VIB, Dept Mol Microbiol, Mol Cell Biol Lab, Louvain, Belgium Univ Antwerp VIB, Dept Mol Genet, Mol Neurogen Grp, B-2610 Antwerp, BelgiumRasic, Vedrana Milic论文数: 0 引用数: 0 h-index: 0机构: Univ Belgrade, Clin Neurol & Psychiat Children & Youth, Belgrade, Serbia Univ Belgrade, Fac Med, Belgrade, Serbia Univ Antwerp VIB, Dept Mol Genet, Mol Neurogen Grp, B-2610 Antwerp, BelgiumJanecke, Andreas R.论文数: 0 引用数: 0 h-index: 0机构: Innsbruck Med Univ, Dept Pediat 2, Innsbruck, Austria Innsbruck Med Univ, Div Human Genet, Innsbruck, Austria Univ Antwerp VIB, Dept Mol Genet, Mol Neurogen Grp, B-2610 Antwerp, BelgiumDe Jonghe, Peter论文数: 0 引用数: 0 h-index: 0机构: Univ Antwerp, Neurogenet Lab, Inst Born Bunge, B-2020 Antwerp, Belgium Univ Antwerp VIB, Dept Mol Genet, Neurogenet Grp, B-2020 Antwerp, Belgium Univ Antwerp Hosp, Dept Neurol, Antwerp, Belgium Univ Antwerp VIB, Dept Mol Genet, Mol Neurogen Grp, B-2610 Antwerp, Belgium论文数: 引用数: h-index:机构:
- [8] Loss-of-function mutations in HINT1 cause axonal neuropathy with neuromyotoniaNature Genetics, 2012, 44 : 1080 - 1083Magdalena Zimoń论文数: 0 引用数: 0 h-index: 0机构: Molecular Neurogenomics Group,Department of Molecular GeneticsJonathan Baets论文数: 0 引用数: 0 h-index: 0机构: Molecular Neurogenomics Group,Department of Molecular GeneticsLeonardo Almeida-Souza论文数: 0 引用数: 0 h-index: 0机构: Molecular Neurogenomics Group,Department of Molecular GeneticsEls De Vriendt论文数: 0 引用数: 0 h-index: 0机构: Molecular Neurogenomics Group,Department of Molecular GeneticsJelena Nikodinovic论文数: 0 引用数: 0 h-index: 0机构: Molecular Neurogenomics Group,Department of Molecular GeneticsYesim Parman论文数: 0 引用数: 0 h-index: 0机构: Molecular Neurogenomics Group,Department of Molecular GeneticsEsra Battaloǧlu论文数: 0 引用数: 0 h-index: 0机构: Molecular Neurogenomics Group,Department of Molecular GeneticsZeliha Matur论文数: 0 引用数: 0 h-index: 0机构: Molecular Neurogenomics Group,Department of Molecular GeneticsVelina Guergueltcheva论文数: 0 引用数: 0 h-index: 0机构: Molecular Neurogenomics Group,Department of Molecular GeneticsIvailo Tournev论文数: 0 引用数: 0 h-index: 0机构: Molecular Neurogenomics Group,Department of Molecular GeneticsMichaela Auer-Grumbach论文数: 0 引用数: 0 h-index: 0机构: Molecular Neurogenomics Group,Department of Molecular GeneticsPeter De Rijk论文数: 0 引用数: 0 h-index: 0机构: Molecular Neurogenomics Group,Department of Molecular GeneticsBritt-Sabina Petersen论文数: 0 引用数: 0 h-index: 0机构: Molecular Neurogenomics Group,Department of Molecular GeneticsThomas Müller论文数: 0 引用数: 0 h-index: 0机构: Molecular Neurogenomics Group,Department of Molecular GeneticsErik Fransen论文数: 0 引用数: 0 h-index: 0机构: Molecular Neurogenomics Group,Department of Molecular GeneticsPhilip Van Damme论文数: 0 引用数: 0 h-index: 0机构: Molecular Neurogenomics Group,Department of Molecular GeneticsWolfgang N Löscher论文数: 0 引用数: 0 h-index: 0机构: Molecular Neurogenomics Group,Department of Molecular GeneticsNina Barišić论文数: 0 引用数: 0 h-index: 0机构: Molecular Neurogenomics Group,Department of Molecular GeneticsZoran Mitrovic论文数: 0 引用数: 0 h-index: 0机构: Molecular Neurogenomics Group,Department of Molecular GeneticsStefano C Previtali论文数: 0 引用数: 0 h-index: 0机构: Molecular Neurogenomics Group,Department of Molecular GeneticsHaluk Topaloǧlu论文数: 0 引用数: 0 h-index: 0机构: Molecular Neurogenomics Group,Department of Molecular GeneticsGünther Bernert论文数: 0 引用数: 0 h-index: 0机构: Molecular Neurogenomics Group,Department of Molecular GeneticsAna Beleza-Meireles论文数: 0 引用数: 0 h-index: 0机构: Molecular Neurogenomics Group,Department of Molecular GeneticsSlobodanka Todorovic论文数: 0 引用数: 0 h-index: 0机构: Molecular Neurogenomics Group,Department of Molecular GeneticsDusanka Savic-Pavicevic论文数: 0 引用数: 0 h-index: 0机构: Molecular Neurogenomics Group,Department of Molecular GeneticsBoryana Ishpekova论文数: 0 引用数: 0 h-index: 0机构: Molecular Neurogenomics Group,Department of Molecular GeneticsSilvia Lechner论文数: 0 引用数: 0 h-index: 0机构: Molecular Neurogenomics Group,Department of Molecular GeneticsKristien Peeters论文数: 0 引用数: 0 h-index: 0机构: Molecular Neurogenomics Group,Department of Molecular GeneticsTinne Ooms论文数: 0 引用数: 0 h-index: 0机构: Molecular Neurogenomics Group,Department of Molecular GeneticsAngelika F Hahn论文数: 0 引用数: 0 h-index: 0机构: Molecular Neurogenomics Group,Department of Molecular GeneticsStephan Züchner论文数: 0 引用数: 0 h-index: 0机构: Molecular Neurogenomics Group,Department of Molecular GeneticsVincent Timmerman论文数: 0 引用数: 0 h-index: 0机构: Molecular Neurogenomics Group,Department of Molecular GeneticsPatrick Van Dijck论文数: 0 引用数: 0 h-index: 0机构: Molecular Neurogenomics Group,Department of Molecular GeneticsVedrana Milic Rasic论文数: 0 引用数: 0 h-index: 0机构: Molecular Neurogenomics Group,Department of Molecular GeneticsAndreas R Janecke论文数: 0 引用数: 0 h-index: 0机构: Molecular Neurogenomics Group,Department of Molecular GeneticsPeter De Jonghe论文数: 0 引用数: 0 h-index: 0机构: Molecular Neurogenomics Group,Department of Molecular GeneticsAlbena Jordanova论文数: 0 引用数: 0 h-index: 0机构: Molecular Neurogenomics Group,Department of Molecular Genetics
- [9] Novel mutations in HINT1 gene cause the autosomal recessive axonal neuropathy with neuromyotoniaJOURNAL OF THE PERIPHERAL NERVOUS SYSTEM, 2018, 23 (04) : 308 - 308Lin, Jie论文数: 0 引用数: 0 h-index: 0机构: Fudan Univ, Huashan Hosp, Dept Neurol, Shanghai, Peoples R China Fudan Univ, Huashan Hosp, Dept Neurol, Shanghai, Peoples R ChinaWang, Zhangyang论文数: 0 引用数: 0 h-index: 0机构: Fudan Univ, Huashan Hosp, Dept Neurol, Shanghai, Peoples R China Fudan Univ, Huashan Hosp, Dept Neurol, Shanghai, Peoples R ChinaLu, Jiahong论文数: 0 引用数: 0 h-index: 0机构: Fudan Univ, Huashan Hosp, Dept Neurol, Shanghai, Peoples R China Fudan Univ, Huashan Hosp, Dept Neurol, Shanghai, Peoples R ChinaZhao, Zhongbo论文数: 0 引用数: 0 h-index: 0机构: Fudan Univ, Huashan Hosp, Dept Neurol, Shanghai, Peoples R China Fudan Univ, Huashan Hosp, Dept Neurol, Shanghai, Peoples R China
- [10] Novel mutations in HINT1 gene cause the autosomal recessive axonal neuropathy with neuromyotoniaEUROPEAN JOURNAL OF MEDICAL GENETICS, 2019, 62 (03) : 190 - 194Wang, Zhangyang论文数: 0 引用数: 0 h-index: 0机构: Fudan Univ, Huashan Hosp, Dept Neurol, Shanghai, Peoples R China Fudan Univ, Huashan Hosp, Dept Neurol, Shanghai, Peoples R ChinaLin, Jie论文数: 0 引用数: 0 h-index: 0机构: Fudan Univ, Huashan Hosp, Dept Neurol, Shanghai, Peoples R China Fudan Univ, Huashan Hosp, Dept Neurol, Shanghai, Peoples R ChinaQiao, Kai论文数: 0 引用数: 0 h-index: 0机构: Fudan Univ, Huashan Hosp, Dept Neurol, Shanghai, Peoples R China Fudan Univ, Huashan Hosp, Dept Neurol, Shanghai, Peoples R ChinaCai, Shuang论文数: 0 引用数: 0 h-index: 0机构: Fudan Univ, Huashan Hosp, Dept Neurol, Shanghai, Peoples R China Fudan Univ, Huashan Hosp, Dept Neurol, Shanghai, Peoples R ChinaZhang, Victor W.论文数: 0 引用数: 0 h-index: 0机构: AmCare Genom Lab, Guangzhou, Guangdong, Peoples R China Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA Fudan Univ, Huashan Hosp, Dept Neurol, Shanghai, Peoples R ChinaZhao, Chongbo论文数: 0 引用数: 0 h-index: 0机构: Fudan Univ, Huashan Hosp, Dept Neurol, Shanghai, Peoples R China Fudan Univ, Huashan Hosp, Dept Neurol, Shanghai, Peoples R ChinaLu, Jiahong论文数: 0 引用数: 0 h-index: 0机构: Fudan Univ, Huashan Hosp, Dept Neurol, Shanghai, Peoples R China Fudan Univ, Huashan Hosp, Dept Neurol, Shanghai, Peoples R China