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- [1] A novel homozygous DJ1 mutation causes parkinsonism and ALS in a Turkish familyPARKINSONISM & RELATED DISORDERS, 2016, 29 : 117 - 120Hanagasi, Hasmet A.论文数: 0 引用数: 0 h-index: 0机构: Istanbul Univ, Istanbul Fac Med, Dept Neurol, Behav Neurol & Movement Disorders Unit, TR-34390 Istanbul, Turkey Istanbul Univ, Istanbul Fac Med, Dept Neurol, Behav Neurol & Movement Disorders Unit, TR-34390 Istanbul, TurkeyGiri, Anamika论文数: 0 引用数: 0 h-index: 0机构: Univ Tubingen, Dept Neurodegenerat Dis, Hertie Inst Clin Brain Res, Tubingen, Germany German Ctr Neurodegenerat Dis, DZNE, Tubingen, Germany Istanbul Univ, Istanbul Fac Med, Dept Neurol, Behav Neurol & Movement Disorders Unit, TR-34390 Istanbul, TurkeyKartal, Ece论文数: 0 引用数: 0 h-index: 0机构: Bogazici Univ, Dept Mol Biol & Genet, Neurodegenerat Res Lab, TR-34342 Istanbul, Turkey Istanbul Univ, Istanbul Fac Med, Dept Neurol, Behav Neurol & Movement Disorders Unit, TR-34390 Istanbul, TurkeyGuven, Gamze论文数: 0 引用数: 0 h-index: 0机构: Istanbul Univ, Inst Expt Med, Dept Genet, Istanbul, Turkey Istanbul Univ, Istanbul Fac Med, Dept Neurol, Behav Neurol & Movement Disorders Unit, TR-34390 Istanbul, TurkeyBilgic, Basar论文数: 0 引用数: 0 h-index: 0机构: Istanbul Univ, Istanbul Fac Med, Dept Neurol, Behav Neurol & Movement Disorders Unit, TR-34390 Istanbul, Turkey Istanbul Univ, Istanbul Fac Med, Dept Neurol, Behav Neurol & Movement Disorders Unit, TR-34390 Istanbul, TurkeyHauser, Ann-Kathrin论文数: 0 引用数: 0 h-index: 0机构: Univ Tubingen, Dept Neurodegenerat Dis, Hertie Inst Clin Brain Res, Tubingen, Germany German Ctr Neurodegenerat Dis, DZNE, Tubingen, Germany Istanbul Univ, Istanbul Fac Med, Dept Neurol, Behav Neurol & Movement Disorders Unit, TR-34390 Istanbul, TurkeyEmre, Murat论文数: 0 引用数: 0 h-index: 0机构: Istanbul Univ, Istanbul Fac Med, Dept Neurol, Behav Neurol & Movement Disorders Unit, TR-34390 Istanbul, Turkey Istanbul Univ, Istanbul Fac Med, Dept Neurol, Behav Neurol & Movement Disorders Unit, TR-34390 Istanbul, TurkeyHeutink, Peter论文数: 0 引用数: 0 h-index: 0机构: Univ Tubingen, Dept Neurodegenerat Dis, Hertie Inst Clin Brain Res, Tubingen, Germany German Ctr Neurodegenerat Dis, DZNE, Tubingen, Germany Istanbul Univ, Istanbul Fac Med, Dept Neurol, Behav Neurol & Movement Disorders Unit, TR-34390 Istanbul, TurkeyBasak, Nazh论文数: 0 引用数: 0 h-index: 0机构: Bogazici Univ, Dept Mol Biol & Genet, Neurodegenerat Res Lab, TR-34342 Istanbul, Turkey Istanbul Univ, Istanbul Fac Med, Dept Neurol, Behav Neurol & Movement Disorders Unit, TR-34390 Istanbul, TurkeyGasser, Thomas论文数: 0 引用数: 0 h-index: 0机构: Univ Tubingen, Dept Neurodegenerat Dis, Hertie Inst Clin Brain Res, Tubingen, Germany German Ctr Neurodegenerat Dis, DZNE, Tubingen, Germany Istanbul Univ, Istanbul Fac Med, Dept Neurol, Behav Neurol & Movement Disorders Unit, TR-34390 Istanbul, TurkeySimon-Sanchez, Javier论文数: 0 引用数: 0 h-index: 0机构: Univ Tubingen, Dept Neurodegenerat Dis, Hertie Inst Clin Brain Res, Tubingen, Germany German Ctr Neurodegenerat Dis, DZNE, Tubingen, Germany Istanbul Univ, Istanbul Fac Med, Dept Neurol, Behav Neurol & Movement Disorders Unit, TR-34390 Istanbul, TurkeyLohmann, Ebba论文数: 0 引用数: 0 h-index: 0机构: Istanbul Univ, Istanbul Fac Med, Dept Neurol, Behav Neurol & Movement Disorders Unit, TR-34390 Istanbul, Turkey Univ Tubingen, Dept Neurodegenerat Dis, Hertie Inst Clin Brain Res, Tubingen, Germany German Ctr Neurodegenerat Dis, DZNE, Tubingen, Germany Istanbul Univ, Istanbul Fac Med, Dept Neurol, Behav Neurol & Movement Disorders Unit, TR-34390 Istanbul, Turkey
- [2] Atypical Parkinsonism-Dystonia Syndrome Caused by a Novel DJ1 MutationMOVEMENT DISORDERS CLINICAL PRACTICE, 2014, 1 (01): : 45 - 49Bras, Jose M.论文数: 0 引用数: 0 h-index: 0机构: UCL, Inst Neurol, Dept Mol Neurosci, London, England UCL, Inst Neurol, Dept Mol Neurosci, London, EnglandGuerreiro, Rita J.论文数: 0 引用数: 0 h-index: 0机构: UCL, Inst Neurol, Dept Mol Neurosci, London, England UCL, Inst Neurol, Dept Mol Neurosci, London, EnglandTeo, James T. H.论文数: 0 引用数: 0 h-index: 0机构: Charing Cross Hosp, Imperial Coll Healthcare NHS Trust, Dept Clin Neurosci, London, England UCL, Inst Neurol, Dept Mol Neurosci, London, EnglandDarwent, Lee论文数: 0 引用数: 0 h-index: 0机构: UCL, Inst Neurol, Dept Mol Neurosci, London, England UCL, Inst Neurol, Dept Mol Neurosci, London, EnglandVaughan, Jenny论文数: 0 引用数: 0 h-index: 0机构: Charing Cross Hosp, Imperial Coll Healthcare NHS Trust, Dept Clin Neurosci, London, England UCL, Inst Neurol, Dept Mol Neurosci, London, EnglandMolloy, Sophie论文数: 0 引用数: 0 h-index: 0机构: Charing Cross Hosp, Imperial Coll Healthcare NHS Trust, Dept Clin Neurosci, London, England UCL, Inst Neurol, Dept Mol Neurosci, London, EnglandHardy, John论文数: 0 引用数: 0 h-index: 0机构: UCL, Inst Neurol, Dept Mol Neurosci, London, England UCL, Inst Neurol, Dept Mol Neurosci, London, EnglandSchneider, Susanne A.论文数: 0 引用数: 0 h-index: 0机构: Charing Cross Hosp, Imperial Coll Healthcare NHS Trust, Dept Clin Neurosci, London, England Univ Kiel, Dept Neurol, Arnold Heller Str 3, D-24105 Kiel, Germany UCL, Inst Neurol, Dept Mol Neurosci, London, England
- [3] A new Turkish family with homozygous FBX07 truncating mutation and juvenile atypical parkinsonismPARKINSONISM & RELATED DISORDERS, 2014, 20 (11) : 1248 - 1252Yalcin-Cakmakli, Gul论文数: 0 引用数: 0 h-index: 0机构: Hacettepe Univ, Dept Neurol, Ankara, Turkey Hacettepe Univ, Dept Neurol, Ankara, TurkeyOlgiati, Simone论文数: 0 引用数: 0 h-index: 0机构: Erasmus MC, Dept Clin Genet, NL-3000 CA Rotterdam, Netherlands Hacettepe Univ, Dept Neurol, Ankara, TurkeyQuadri, Marialuisa论文数: 0 引用数: 0 h-index: 0机构: Erasmus MC, Dept Clin Genet, NL-3000 CA Rotterdam, Netherlands Hacettepe Univ, Dept Neurol, Ankara, TurkeyBreedveld, Guido J.论文数: 0 引用数: 0 h-index: 0机构: Erasmus MC, Dept Clin Genet, NL-3000 CA Rotterdam, Netherlands Hacettepe Univ, Dept Neurol, Ankara, Turkey论文数: 引用数: h-index:机构:Bonifati, Vincenzo论文数: 0 引用数: 0 h-index: 0机构: Erasmus MC, Dept Clin Genet, NL-3000 CA Rotterdam, Netherlands Hacettepe Univ, Dept Neurol, Ankara, TurkeyElibol, Bulent论文数: 0 引用数: 0 h-index: 0机构: Hacettepe Univ, Dept Neurol, Ankara, Turkey Hacettepe Univ, Dept Neurol, Ankara, Turkey
- [4] Novel homozygous p.E64D mutation in DJ1 in early onset Parkinson disease (PARK7)HUMAN MUTATION, 2004, 24 (04) : 321 - 329Hering, R论文数: 0 引用数: 0 h-index: 0机构: Univ Tubingen, Dept Med Genet, D-72076 Tubingen, GermanyStrauss, KA论文数: 0 引用数: 0 h-index: 0机构: Univ Tubingen, Dept Med Genet, D-72076 Tubingen, GermanyTao, X论文数: 0 引用数: 0 h-index: 0机构: Univ Tubingen, Dept Med Genet, D-72076 Tubingen, GermanyBauer, A论文数: 0 引用数: 0 h-index: 0机构: Univ Tubingen, Dept Med Genet, D-72076 Tubingen, GermanyWoitalla, D论文数: 0 引用数: 0 h-index: 0机构: Univ Tubingen, Dept Med Genet, D-72076 Tubingen, GermanyMietz, EM论文数: 0 引用数: 0 h-index: 0机构: Univ Tubingen, Dept Med Genet, D-72076 Tubingen, GermanyBauer, P论文数: 0 引用数: 0 h-index: 0机构: Univ Tubingen, Dept Med Genet, D-72076 Tubingen, GermanySchaible, JB论文数: 0 引用数: 0 h-index: 0机构: Univ Tubingen, Dept Med Genet, D-72076 Tubingen, GermanyMüller, T论文数: 0 引用数: 0 h-index: 0机构: Univ Tubingen, Dept Med Genet, D-72076 Tubingen, GermanySchöls, L论文数: 0 引用数: 0 h-index: 0机构: Univ Tubingen, Dept Med Genet, D-72076 Tubingen, GermanyKlein, C论文数: 0 引用数: 0 h-index: 0机构: Univ Tubingen, Dept Med Genet, D-72076 Tubingen, GermanyBerg, D论文数: 0 引用数: 0 h-index: 0机构: Univ Tubingen, Dept Med Genet, D-72076 Tubingen, GermanyMeyer, PT论文数: 0 引用数: 0 h-index: 0机构: Univ Tubingen, Dept Med Genet, D-72076 Tubingen, GermanySchulz, JB论文数: 0 引用数: 0 h-index: 0机构: Univ Tubingen, Dept Med Genet, D-72076 Tubingen, GermanyWollnik, B论文数: 0 引用数: 0 h-index: 0机构: Univ Tubingen, Dept Med Genet, D-72076 Tubingen, GermanyTong, L论文数: 0 引用数: 0 h-index: 0机构: Univ Tubingen, Dept Med Genet, D-72076 Tubingen, GermanyKrüger, R论文数: 0 引用数: 0 h-index: 0机构: Univ Tubingen, Dept Med Genet, D-72076 Tubingen, GermanyRiess, O论文数: 0 引用数: 0 h-index: 0机构: Univ Tubingen, Dept Med Genet, D-72076 Tubingen, Germany
- [5] A novel homozygous HOXB1 mutation in a Turkish family with hereditary congenital facial paresisBRAIN & DEVELOPMENT, 2017, 39 (02): : 166 - 170Sahin, Yavuz论文数: 0 引用数: 0 h-index: 0机构: Necip Fazil City Hosp, Dept Med Genet, Kahramanmaras, Turkey Necip Fazil City Hosp, Dept Med Genet, Kahramanmaras, TurkeyGungor, Olcay论文数: 0 引用数: 0 h-index: 0机构: Necip Fazil City Hosp, Dept Pediat Neurol, Kahramanmaras, Turkey Necip Fazil City Hosp, Dept Med Genet, Kahramanmaras, TurkeyAyaz, Akif论文数: 0 引用数: 0 h-index: 0机构: Adana Res & Training Hosp, Dept Med Genet, Adana, Turkey Necip Fazil City Hosp, Dept Med Genet, Kahramanmaras, TurkeyGungor, Gulay论文数: 0 引用数: 0 h-index: 0机构: Kahramanmaras Sutcu Imam Univ, Dept Radiol, Fac Med, Kahramanmaras, Turkey Necip Fazil City Hosp, Dept Med Genet, Kahramanmaras, TurkeySahin, Bedia论文数: 0 引用数: 0 h-index: 0机构: Kahramanmaras Sutcu Imam Univ, Dept Ophthalmol, Fac Med, Kahramanmaras, Turkey Necip Fazil City Hosp, Dept Med Genet, Kahramanmaras, TurkeyYaykasli, Kursad论文数: 0 引用数: 0 h-index: 0机构: Kahramanmaras Sutcu Imam Univ, Dept Med Biol, Kahramanmaras, Turkey Necip Fazil City Hosp, Dept Med Genet, Kahramanmaras, TurkeyCeylaner, Serdar论文数: 0 引用数: 0 h-index: 0机构: Intergen Lab, Dept Med Genet, Ankara, Turkey Necip Fazil City Hosp, Dept Med Genet, Kahramanmaras, Turkey
- [6] Young-onset SOD1-ALS caused by a novel homozygous mutation, a family reportNEUROMUSCULAR DISORDERS, 2021, 31 : S123 - S123论文数: 引用数: h-index:机构:Mueller, K.论文数: 0 引用数: 0 h-index: 0机构: Univ Ulm, Ulm, Germany Ain Shams Univ, Cairo, EgyptAndersen, P.论文数: 0 引用数: 0 h-index: 0机构: Umea Univ, Umea, Sweden Ain Shams Univ, Cairo, EgyptMarklund, S.论文数: 0 引用数: 0 h-index: 0机构: Umea Univ, Umea, Sweden Ain Shams Univ, Cairo, EgyptLudolph, A.论文数: 0 引用数: 0 h-index: 0机构: Univ Ulm, Ulm, Germany Ain Shams Univ, Cairo, EgyptHamdi, N.论文数: 0 引用数: 0 h-index: 0机构: German Univ Cairo, Cairo, Egypt Ain Shams Univ, Cairo, Egypt
- [7] A novel homozygous PLA2G6 mutation causes dystonia-parkinsonismPARKINSONISM & RELATED DISORDERS, 2015, 21 (03) : 337 - 339Malaguti, M. C.论文数: 0 引用数: 0 h-index: 0机构: Santa Chiara Hosp, Dept Neurol, Trento, Italy Santa Chiara Hosp, Dept Neurol, Trento, ItalyMelzi, V.论文数: 0 引用数: 0 h-index: 0机构: Univ Milan, Dept Pathophysiol & Transplantat, IRCCS Fdn Ca Granda Osped Maggiore Policlin, Dino Ferrari Ctr,Neurosci Sect, Milan, Italy Santa Chiara Hosp, Dept Neurol, Trento, ItalyDi Giacopo, R.论文数: 0 引用数: 0 h-index: 0机构: Univ Trento, Ctr Mind Brain Sci CIMEC, Ctr Riabilitaz Neurocognit CeRiN, Trento, Italy Santa Chiara Hosp, Dept Neurol, Trento, ItalyMonfrini, E.论文数: 0 引用数: 0 h-index: 0机构: Univ Milan, Dept Pathophysiol & Transplantat, IRCCS Fdn Ca Granda Osped Maggiore Policlin, Dino Ferrari Ctr,Neurosci Sect, Milan, Italy Santa Chiara Hosp, Dept Neurol, Trento, ItalyDi Biase, E.论文数: 0 引用数: 0 h-index: 0机构: Univ Milan, Dept Pathophysiol & Transplantat, IRCCS Fdn Ca Granda Osped Maggiore Policlin, Dino Ferrari Ctr,Neurosci Sect, Milan, Italy Santa Chiara Hosp, Dept Neurol, Trento, ItalyFranco, G.论文数: 0 引用数: 0 h-index: 0机构: Univ Milan, Dept Pathophysiol & Transplantat, IRCCS Fdn Ca Granda Osped Maggiore Policlin, Dino Ferrari Ctr,Neurosci Sect, Milan, Italy Santa Chiara Hosp, Dept Neurol, Trento, Italy论文数: 引用数: h-index:机构:论文数: 引用数: h-index:机构:Compagnoni, G. Monzio论文数: 0 引用数: 0 h-index: 0机构: Univ Milan, Dept Pathophysiol & Transplantat, IRCCS Fdn Ca Granda Osped Maggiore Policlin, Dino Ferrari Ctr,Neurosci Sect, Milan, Italy Santa Chiara Hosp, Dept Neurol, Trento, ItalyFortis, P.论文数: 0 引用数: 0 h-index: 0机构: Univ Trento, Ctr Mind Brain Sci CIMEC, Ctr Riabilitaz Neurocognit CeRiN, Trento, Italy Santa Chiara Hosp, Dept Neurol, Trento, ItalyFeraco, P.论文数: 0 引用数: 0 h-index: 0机构: Santa Chiara Hosp, Dept Radiol, SS Neuroradiol, Trento, Italy Santa Chiara Hosp, Dept Neurol, Trento, ItalyOrrico, D.论文数: 0 引用数: 0 h-index: 0机构: Santa Chiara Hosp, Dept Neurol, Trento, Italy Santa Chiara Hosp, Dept Neurol, Trento, ItalyCucurachi, L.论文数: 0 引用数: 0 h-index: 0机构: Santa Chiara Hosp, Dept Neurol, Trento, Italy Santa Chiara Hosp, Dept Neurol, Trento, ItalyDonner, D.论文数: 0 引用数: 0 h-index: 0机构: Santa Chiara Hosp, Dept Nucl Med, Trento, Italy Santa Chiara Hosp, Dept Neurol, Trento, ItalyRizzuti, M.论文数: 0 引用数: 0 h-index: 0机构: Univ Milan, Dept Pathophysiol & Transplantat, IRCCS Fdn Ca Granda Osped Maggiore Policlin, Dino Ferrari Ctr,Neurosci Sect, Milan, Italy Santa Chiara Hosp, Dept Neurol, Trento, ItalyRonchi, D.论文数: 0 引用数: 0 h-index: 0机构: Univ Milan, Dept Pathophysiol & Transplantat, IRCCS Fdn Ca Granda Osped Maggiore Policlin, Dino Ferrari Ctr,Neurosci Sect, Milan, Italy Santa Chiara Hosp, Dept Neurol, Trento, ItalyBonato, S.论文数: 0 引用数: 0 h-index: 0机构: Univ Milan, Dept Pathophysiol & Transplantat, IRCCS Fdn Ca Granda Osped Maggiore Policlin, Dino Ferrari Ctr,Neurosci Sect, Milan, Italy Santa Chiara Hosp, Dept Neurol, Trento, Italy论文数: 引用数: h-index:机构:Corti, S.论文数: 0 引用数: 0 h-index: 0机构: Univ Milan, Dept Pathophysiol & Transplantat, IRCCS Fdn Ca Granda Osped Maggiore Policlin, Dino Ferrari Ctr,Neurosci Sect, Milan, Italy Santa Chiara Hosp, Dept Neurol, Trento, ItalyComi, G. P.论文数: 0 引用数: 0 h-index: 0机构: Univ Milan, Dept Pathophysiol & Transplantat, IRCCS Fdn Ca Granda Osped Maggiore Policlin, Dino Ferrari Ctr,Neurosci Sect, Milan, Italy Santa Chiara Hosp, Dept Neurol, Trento, ItalyDi Fonzo, A.论文数: 0 引用数: 0 h-index: 0机构: Univ Milan, Dept Pathophysiol & Transplantat, IRCCS Fdn Ca Granda Osped Maggiore Policlin, Dino Ferrari Ctr,Neurosci Sect, Milan, Italy Santa Chiara Hosp, Dept Neurol, Trento, Italy
- [8] Identification of a novel homozygous TBC1D24 mutation in a Turkish family with DOORS syndromeCLINICAL DYSMORPHOLOGY, 2018, 27 (01) : 1 - 3Atli, Engin论文数: 0 引用数: 0 h-index: 0机构: Trakya Univ, Fac Med, Dept Med Genet, TR-22030 Edirne, Turkey Trakya Univ, Fac Med, Dept Med Genet, TR-22030 Edirne, TurkeyGurkan, Hakan论文数: 0 引用数: 0 h-index: 0机构: Trakya Univ, Fac Med, Dept Med Genet, TR-22030 Edirne, Turkey Trakya Univ, Fac Med, Dept Med Genet, TR-22030 Edirne, TurkeyUlusal, Selma论文数: 0 引用数: 0 h-index: 0机构: Trakya Univ, Fac Med, Dept Med Genet, TR-22030 Edirne, Turkey Trakya Univ, Fac Med, Dept Med Genet, TR-22030 Edirne, TurkeyKaral, Yasemin论文数: 0 引用数: 0 h-index: 0机构: Trakya Univ, Fac Med, Dept Pediat, Edirne, Turkey Trakya Univ, Fac Med, Dept Med Genet, TR-22030 Edirne, TurkeyAtli, Emine I.论文数: 0 引用数: 0 h-index: 0机构: Trakya Univ, Fac Med, Dept Med Genet, TR-22030 Edirne, Turkey Trakya Univ, Fac Med, Dept Med Genet, TR-22030 Edirne, TurkeyTozkir, Hilmi论文数: 0 引用数: 0 h-index: 0机构: Trakya Univ, Fac Med, Dept Med Genet, TR-22030 Edirne, Turkey Trakya Univ, Fac Med, Dept Med Genet, TR-22030 Edirne, Turkey
- [9] Novel homozygous KREMEN1 mutation causes ectodermal dysplasiaORAL DISEASES, 2022, 28 (03) : 843 - 845Lee, Yejin论文数: 0 引用数: 0 h-index: 0机构: Seoul Natl Univ, Sch Dent, Dept Pediat Dent, 101 Daehak Ro, Seoul 03080, South Korea Seoul Natl Univ, DRI, 101 Daehak Ro, Seoul 03080, South Korea Seoul Natl Univ, Sch Dent, Dept Pediat Dent, 101 Daehak Ro, Seoul 03080, South KoreaZhang, Hong论文数: 0 引用数: 0 h-index: 0机构: Univ Michigan, Sch Dent, Dept Biol & Mat Sci, Ann Arbor, MI 48109 USA Seoul Natl Univ, Sch Dent, Dept Pediat Dent, 101 Daehak Ro, Seoul 03080, South KoreaSeymen, Figen论文数: 0 引用数: 0 h-index: 0机构: Istanbul Univ, Fac Dent, Dept Pedodont, Istanbul, Turkey Seoul Natl Univ, Sch Dent, Dept Pediat Dent, 101 Daehak Ro, Seoul 03080, South KoreaKoruyucu, Mine论文数: 0 引用数: 0 h-index: 0机构: Istanbul Univ, Fac Dent, Dept Pedodont, Istanbul, Turkey Seoul Natl Univ, Sch Dent, Dept Pediat Dent, 101 Daehak Ro, Seoul 03080, South KoreaKasimoglu, Yelda论文数: 0 引用数: 0 h-index: 0机构: Istanbul Univ, Fac Dent, Dept Pedodont, Istanbul, Turkey Seoul Natl Univ, Sch Dent, Dept Pediat Dent, 101 Daehak Ro, Seoul 03080, South KoreaLee, Zang Hee论文数: 0 引用数: 0 h-index: 0机构: Seoul Natl Univ, DRI, 101 Daehak Ro, Seoul 03080, South Korea Seoul Natl Univ, Sch Dent, Dept Cell & Dev Biol, Seoul, South Korea Seoul Natl Univ, Sch Dent, Dept Pediat Dent, 101 Daehak Ro, Seoul 03080, South KoreaHu, Jan C. -C.论文数: 0 引用数: 0 h-index: 0机构: Univ Michigan, Sch Dent, Dept Biol & Mat Sci, Ann Arbor, MI 48109 USA Seoul Natl Univ, Sch Dent, Dept Pediat Dent, 101 Daehak Ro, Seoul 03080, South KoreaSimmer, James P.论文数: 0 引用数: 0 h-index: 0机构: Univ Michigan, Sch Dent, Dept Biol & Mat Sci, Ann Arbor, MI 48109 USA Seoul Natl Univ, Sch Dent, Dept Pediat Dent, 101 Daehak Ro, Seoul 03080, South KoreaKim, Jung-Wook论文数: 0 引用数: 0 h-index: 0机构: Seoul Natl Univ, Sch Dent, Dept Pediat Dent, 101 Daehak Ro, Seoul 03080, South Korea Seoul Natl Univ, DRI, 101 Daehak Ro, Seoul 03080, South Korea Seoul Natl Univ, Sch Dent, Dept Mol Genet, 101 Daehak Ro, Seoul 03080, South Korea Seoul Natl Univ, Sch Dent, Dept Pediat Dent, 101 Daehak Ro, Seoul 03080, South Korea
- [10] GNE Myopathy in Turkish Sisters with a Novel Homozygous MutationCASE REPORTS IN NEUROLOGICAL MEDICINE, 2016, 2016Diniz, Gulden论文数: 0 引用数: 0 h-index: 0机构: Tepecik Res & Training Hosp, Neuromuscular Dis Ctr, Dept Pathol, Izmir, Turkey Tepecik Res & Training Hosp, Neuromuscular Dis Ctr, Dept Pathol, Izmir, TurkeySecil, Yaprak论文数: 0 引用数: 0 h-index: 0机构: Ataturk Training & Res Hosp, Dept Neurol, Izmir, Turkey Tepecik Res & Training Hosp, Neuromuscular Dis Ctr, Dept Pathol, Izmir, TurkeyCeylaner, Serdar论文数: 0 引用数: 0 h-index: 0机构: Intergen Lab, Dept Med Genet, Ankara, Turkey Tepecik Res & Training Hosp, Neuromuscular Dis Ctr, Dept Pathol, Izmir, TurkeyTokucoglu, Figen论文数: 0 引用数: 0 h-index: 0机构: Tepecik Res & Training Hosp, Dept Neurol, Neuromuscular Dis Ctr, Izmir, Turkey Tepecik Res & Training Hosp, Neuromuscular Dis Ctr, Dept Pathol, Izmir, TurkeyTure, Sabiha论文数: 0 引用数: 0 h-index: 0机构: Katip Celebi Univ, Dept Neurol, Izmir, Turkey Tepecik Res & Training Hosp, Neuromuscular Dis Ctr, Dept Pathol, Izmir, TurkeyCelebisoy, Mehmet论文数: 0 引用数: 0 h-index: 0机构: Ataturk Training & Res Hosp, Dept Neurol, Izmir, Turkey Tepecik Res & Training Hosp, Neuromuscular Dis Ctr, Dept Pathol, Izmir, TurkeyEncesu, Tulay Kurt论文数: 0 引用数: 0 h-index: 0机构: Katip Celebi Univ, Dept Neurol, Izmir, Turkey Tepecik Res & Training Hosp, Neuromuscular Dis Ctr, Dept Pathol, Izmir, TurkeyAkhan, Galip论文数: 0 引用数: 0 h-index: 0机构: Katip Celebi Univ, Dept Neurol, Izmir, Turkey Tepecik Res & Training Hosp, Neuromuscular Dis Ctr, Dept Pathol, Izmir, Turkey