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- [41] A missense mutation in LIM2 causes autosomal recessive congenital cataractMOLECULAR VISION, 2008, 14 (141): : 1204 - 1208Ponnam, Surya Prakash G.论文数: 0 引用数: 0 h-index: 0机构: Hyderabad Eye Res Fdn, Champalimaud Translat Ctr, Kallam Anji Reddy Mol Genet Lab, LV Prasad Eye Inst,Brien Holden Eye Res Ctr,HERF, Hyderabad 500034, Andhra Pradesh, IndiaRamesha, Kekunnaya论文数: 0 引用数: 0 h-index: 0机构: LV Prasad Eye Inst, Jasti V Ramanamma Childrens Eye Care Ctr, Hyderabad, Andhra Pradesh, India Hyderabad Eye Res Fdn, Champalimaud Translat Ctr, Kallam Anji Reddy Mol Genet Lab, LV Prasad Eye Inst,Brien Holden Eye Res Ctr,HERF, Hyderabad 500034, Andhra Pradesh, IndiaTejwani, Sushma论文数: 0 引用数: 0 h-index: 0机构: LV Prasad Eye Inst, Jasti V Ramanamma Childrens Eye Care Ctr, Hyderabad, Andhra Pradesh, India Hyderabad Eye Res Fdn, Champalimaud Translat Ctr, Kallam Anji Reddy Mol Genet Lab, LV Prasad Eye Inst,Brien Holden Eye Res Ctr,HERF, Hyderabad 500034, Andhra Pradesh, IndiaMatalia, Jyoti论文数: 0 引用数: 0 h-index: 0机构: LV Prasad Eye Inst, Jasti V Ramanamma Childrens Eye Care Ctr, Hyderabad, Andhra Pradesh, India Hyderabad Eye Res Fdn, Champalimaud Translat Ctr, Kallam Anji Reddy Mol Genet Lab, LV Prasad Eye Inst,Brien Holden Eye Res Ctr,HERF, Hyderabad 500034, Andhra Pradesh, IndiaKannabiran, Chitra论文数: 0 引用数: 0 h-index: 0机构: Hyderabad Eye Res Fdn, Champalimaud Translat Ctr, Kallam Anji Reddy Mol Genet Lab, LV Prasad Eye Inst,Brien Holden Eye Res Ctr,HERF, Hyderabad 500034, Andhra Pradesh, India Hyderabad Eye Res Fdn, Champalimaud Translat Ctr, Kallam Anji Reddy Mol Genet Lab, LV Prasad Eye Inst,Brien Holden Eye Res Ctr,HERF, Hyderabad 500034, Andhra Pradesh, India
- [42] A novel non sense mutation in WDR62 causes autosomal recessive primary microcephaly: a case reportBMC MEDICAL GENETICS, 2018, 19Jaouad, Imane Cherkaoui论文数: 0 引用数: 0 h-index: 0机构: Univ Mohammed 5, Fac Med & Pharm, Ctr Genom Humaine, Rabat, Morocco Inst Natl Hyg, Dept Genet Med, Rabat, Morocco Univ Mohammed 5, Fac Med & Pharm, Ctr Genom Humaine, Rabat, MoroccoZrhidri, Abdelali论文数: 0 引用数: 0 h-index: 0机构: Univ Mohammed 5, Fac Med & Pharm, Ctr Genom Humaine, Rabat, Morocco Univ Mohammed 5, Fac Med & Pharm, Ctr Genom Humaine, Rabat, MoroccoJdioui, Wafaa论文数: 0 引用数: 0 h-index: 0机构: Univ Mohammed 5, Fac Med & Pharm, Ctr Genom Humaine, Rabat, Morocco Inst Natl Hyg, Dept Genet Med, Rabat, Morocco Univ Mohammed 5, Fac Med & Pharm, Ctr Genom Humaine, Rabat, MoroccoLyahyai, Jaber论文数: 0 引用数: 0 h-index: 0机构: Univ Mohammed 5, Fac Med & Pharm, Ctr Genom Humaine, Rabat, Morocco Univ Mohammed 5, Fac Med & Pharm, Ctr Genom Humaine, Rabat, MoroccoRaymond, Laure论文数: 0 引用数: 0 h-index: 0机构: Dept Genet Mol, Lab Biomnis, Lyon, France Univ Mohammed 5, Fac Med & Pharm, Ctr Genom Humaine, Rabat, MoroccoEgea, Gregory论文数: 0 引用数: 0 h-index: 0机构: Dept Genet Mol, Lab Biomnis, Lyon, France Univ Mohammed 5, Fac Med & Pharm, Ctr Genom Humaine, Rabat, MoroccoTaoudi, Mohamed论文数: 0 引用数: 0 h-index: 0机构: Dept Genet Mol, Lab Biomnis, Lyon, France Univ Mohammed 5, Fac Med & Pharm, Ctr Genom Humaine, Rabat, MoroccoEl Mouatassim, Said论文数: 0 引用数: 0 h-index: 0机构: Dept Genet Mol, Lab Biomnis, Lyon, France Univ Mohammed 5, Fac Med & Pharm, Ctr Genom Humaine, Rabat, MoroccoSefiani, Abdelaziz论文数: 0 引用数: 0 h-index: 0机构: Univ Mohammed 5, Fac Med & Pharm, Ctr Genom Humaine, Rabat, Morocco Inst Natl Hyg, Dept Genet Med, Rabat, Morocco Univ Mohammed 5, Fac Med & Pharm, Ctr Genom Humaine, Rabat, Morocco
- [43] A novel desmin mutation causes autosomal recessive limb girdle muscular dystrophy without features of myofibrillar myopathyNEUROMUSCULAR DISORDERS, 2013, 23 (9-10) : 851 - 852Cetin, N.论文数: 0 引用数: 0 h-index: 0机构: Hacettepe Univ, Fac Med, Dept Med Biol, TR-06100 Ankara, Turkey Hacettepe Univ, Fac Med, Dept Med Biol, TR-06100 Ankara, TurkeyBalci-Hayta, B.论文数: 0 引用数: 0 h-index: 0机构: Hacettepe Univ, Fac Med, Dept Med Biol, TR-06100 Ankara, Turkey Hacettepe Univ, Fac Med, Dept Med Biol, TR-06100 Ankara, TurkeyGundesli, H.论文数: 0 引用数: 0 h-index: 0机构: Hacettepe Univ, Fac Med, Dept Med Biol, TR-06100 Ankara, Turkey Hacettepe Univ, Fac Med, Dept Med Biol, TR-06100 Ankara, TurkeyKorkusuz, P.论文数: 0 引用数: 0 h-index: 0机构: Hacettepe Univ, Fac Med, Dept Histol & Embryol, TR-06100 Ankara, Turkey Hacettepe Univ, Fac Med, Dept Med Biol, TR-06100 Ankara, Turkey论文数: 引用数: h-index:机构:Talim, B.论文数: 0 引用数: 0 h-index: 0机构: Hacettepe Univ, Fac Med, Dept Pediat, Pathol Unit, TR-06100 Ankara, Turkey Hacettepe Univ, Fac Med, Dept Med Biol, TR-06100 Ankara, TurkeyTan, E.论文数: 0 引用数: 0 h-index: 0机构: Hacettepe Univ, Fac Med, Dept Neurol, TR-06100 Ankara, Turkey Hacettepe Univ, Fac Med, Neuromuscular Dis Res Lab, TR-06100 Ankara, Turkey Hacettepe Univ, Fac Med, Dept Med Biol, TR-06100 Ankara, TurkeySelcen, D.论文数: 0 引用数: 0 h-index: 0机构: Mayo Clin, Dept Neurol, Rochester, MN USA Mayo Clin, Neuromuscular Dis Res Lab, Rochester, MN USA Hacettepe Univ, Fac Med, Dept Med Biol, TR-06100 Ankara, TurkeyErdem-Ozdamar, S.论文数: 0 引用数: 0 h-index: 0机构: Hacettepe Univ, Fac Med, Dept Neurol, TR-06100 Ankara, Turkey Hacettepe Univ, Fac Med, Neuromuscular Dis Res Lab, TR-06100 Ankara, Turkey Hacettepe Univ, Fac Med, Dept Med Biol, TR-06100 Ankara, TurkeyDincer, P.论文数: 0 引用数: 0 h-index: 0机构: Hacettepe Univ, Fac Med, Dept Med Biol, TR-06100 Ankara, Turkey Hacettepe Univ, Fac Med, Dept Med Biol, TR-06100 Ankara, Turkey
- [44] A Novel Mutation in PYCR1 Causes an Autosomal Recessive Cutis Laxa With Premature Aging Features in a FamilyAMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2011, 155A (06) : 1285 - 1289Lin, Dar-Shong论文数: 0 引用数: 0 h-index: 0机构: Mackay Mem Hosp, Dept Pediat, Taipei, Taiwan Mackay Mem Hosp, Dept Med Res, Taipei, Taiwan Mackay Med Nursing & Management Coll, Taipei, Taiwan Natl Taipei Univ Technol, Dept Chem Engn & Biotechnol, Taipei, Taiwan Mackay Mem Hosp, Dept Pediat, Taipei, TaiwanYeung, Chun-Yan论文数: 0 引用数: 0 h-index: 0机构: Mackay Mem Hosp, Dept Pediat, Taipei, Taiwan Mackay Med Nursing & Management Coll, Taipei, Taiwan Natl Taipei Univ Technol, Dept Chem Engn & Biotechnol, Taipei, Taiwan Mackay Mem Hosp, Dept Pediat, Taipei, TaiwanLiu, Hsuan-Liang论文数: 0 引用数: 0 h-index: 0机构: Natl Taipei Univ Technol, Dept Chem Engn & Biotechnol, Taipei, Taiwan Mackay Mem Hosp, Dept Pediat, Taipei, TaiwanHo, Che-Sheng论文数: 0 引用数: 0 h-index: 0机构: Mackay Mem Hosp, Dept Pediat, Taipei, Taiwan Mackay Mem Hosp, Dept Pediat, Taipei, TaiwanShu, Chyong-Hsin论文数: 0 引用数: 0 h-index: 0机构: Mackay Mem Hosp, Dept Pediat, Taipei, Taiwan Mackay Mem Hosp, Dept Pediat, Taipei, TaiwanChuang, Chih-Kuang论文数: 0 引用数: 0 h-index: 0机构: Mackay Mem Hosp, Dept Med Res, Taipei, Taiwan Natl Taipei Univ Technol, Dept Chem Engn & Biotechnol, Taipei, Taiwan Mackay Mem Hosp, Dept Pediat, Taipei, TaiwanHuang, Yu-Wen论文数: 0 引用数: 0 h-index: 0机构: Mackay Mem Hosp, Dept Med Res, Taipei, Taiwan Mackay Mem Hosp, Dept Pediat, Taipei, TaiwanWu, Tsu-Yen论文数: 0 引用数: 0 h-index: 0机构: Mackay Mem Hosp, Dept Med Res, Taipei, Taiwan Mackay Mem Hosp, Dept Pediat, Taipei, TaiwanHuang, Zon-Darr论文数: 0 引用数: 0 h-index: 0机构: Mackay Mem Hosp, Dept Med Res, Taipei, Taiwan Mackay Mem Hosp, Dept Pediat, Taipei, TaiwanJian, Yuan-Ren论文数: 0 引用数: 0 h-index: 0机构: Mackay Mem Hosp, Dept Med Res, Taipei, Taiwan Mackay Mem Hosp, Dept Pediat, Taipei, TaiwanLin, Shuan-Pei论文数: 0 引用数: 0 h-index: 0机构: Mackay Mem Hosp, Dept Pediat, Taipei, Taiwan Mackay Med Nursing & Management Coll, Taipei, Taiwan Mackay Mem Hosp, Dept Pediat, Taipei, Taiwan
- [45] Neurofascin (NFASC) gene mutation causes autosomal recessive ataxia with demyelinating neuropathyPARKINSONISM & RELATED DISORDERS, 2019, 63 : 66 - 72Monfrini, Edoardo论文数: 0 引用数: 0 h-index: 0机构: Fdn IRCCS Ca Granda Osped Maggiore Policlin, Neurol Unit, Via Francesco Sforza 35, I-20122 Milan, Italy Univ Milan, Neurosci Sect, Dept Pathophysiol & Transplantat, Dino Ferrari Ctr, Milan, Italy Fdn IRCCS Ca Granda Osped Maggiore Policlin, Neurol Unit, Via Francesco Sforza 35, I-20122 Milan, ItalyStraniero, Letizia论文数: 0 引用数: 0 h-index: 0机构: Humanitas Univ, Dept Biomed Sci, Milan, Italy Humanitas Clin & Res Ctr, Milan, Italy Fdn IRCCS Ca Granda Osped Maggiore Policlin, Neurol Unit, Via Francesco Sforza 35, I-20122 Milan, ItalyBonato, Sara论文数: 0 引用数: 0 h-index: 0机构: Fdn IRCCS Ca Granda Osped Maggiore Policlin, Neurol Unit, Via Francesco Sforza 35, I-20122 Milan, Italy Univ Milan, Neurosci Sect, Dept Pathophysiol & Transplantat, Dino Ferrari Ctr, Milan, Italy Fdn IRCCS Ca Granda Osped Maggiore Policlin, Neurol Unit, Via Francesco Sforza 35, I-20122 Milan, ItalyCompagnoni, Giacomo Monzio论文数: 0 引用数: 0 h-index: 0机构: Fdn IRCCS Ca Granda Osped Maggiore Policlin, Neurol Unit, Via Francesco Sforza 35, I-20122 Milan, Italy Univ Milan, Neurosci Sect, Dept Pathophysiol & Transplantat, Dino Ferrari Ctr, Milan, Italy Fdn IRCCS Ca Granda Osped Maggiore Policlin, Neurol Unit, Via Francesco Sforza 35, I-20122 Milan, ItalyBordoni, Andreina论文数: 0 引用数: 0 h-index: 0机构: Fdn IRCCS Ca Granda Osped Maggiore Policlin, Neurol Unit, Via Francesco Sforza 35, I-20122 Milan, Italy Univ Milan, Neurosci Sect, Dept Pathophysiol & Transplantat, Dino Ferrari Ctr, Milan, Italy Fdn IRCCS Ca Granda Osped Maggiore Policlin, Neurol Unit, Via Francesco Sforza 35, I-20122 Milan, ItalyDilena, Robertino论文数: 0 引用数: 0 h-index: 0机构: Fdn IRCCS Ca Granda Osped Maggiore Policlin, Neurofisiopatol Pediat, UOC Neurofisiopatol, Milan, Italy Fdn IRCCS Ca Granda Osped Maggiore Policlin, Neurol Unit, Via Francesco Sforza 35, I-20122 Milan, ItalyRinchetti, Paola论文数: 0 引用数: 0 h-index: 0机构: Fdn IRCCS Ca Granda Osped Maggiore Policlin, Neurol Unit, Via Francesco Sforza 35, I-20122 Milan, Italy Univ Milan, Neurosci Sect, Dept Pathophysiol & Transplantat, Dino Ferrari Ctr, Milan, Italy Fdn IRCCS Ca Granda Osped Maggiore Policlin, Neurol Unit, Via Francesco Sforza 35, I-20122 Milan, ItalySilipigni, Rosamaria论文数: 0 引用数: 0 h-index: 0机构: Fdn IRCCS Ca Granda Osped Maggiore Policlin, Med Genet Lab, Milan, Italy Fdn IRCCS Ca Granda Osped Maggiore Policlin, Neurol Unit, Via Francesco Sforza 35, I-20122 Milan, ItalyRonchi, Dario论文数: 0 引用数: 0 h-index: 0机构: Fdn IRCCS Ca Granda Osped Maggiore Policlin, Neurol Unit, Via Francesco Sforza 35, I-20122 Milan, Italy Univ Milan, Neurosci Sect, Dept Pathophysiol & Transplantat, Dino Ferrari Ctr, Milan, Italy Fdn IRCCS Ca Granda Osped Maggiore Policlin, Neurol Unit, Via Francesco Sforza 35, I-20122 Milan, ItalyCorti, Stefania论文数: 0 引用数: 0 h-index: 0机构: Fdn IRCCS Ca Granda Osped Maggiore Policlin, Neurol Unit, Via Francesco Sforza 35, I-20122 Milan, Italy Univ Milan, Neurosci Sect, Dept Pathophysiol & Transplantat, Dino Ferrari Ctr, Milan, Italy Fdn IRCCS Ca Granda Osped Maggiore Policlin, Neurol Unit, Via Francesco Sforza 35, I-20122 Milan, ItalyComi, Giacomo P.论文数: 0 引用数: 0 h-index: 0机构: Fdn IRCCS Ca Granda Osped Maggiore Policlin, Neurol Unit, Via Francesco Sforza 35, I-20122 Milan, Italy Univ Milan, Neurosci Sect, Dept Pathophysiol & Transplantat, Dino Ferrari Ctr, Milan, Italy Fdn IRCCS Ca Granda Osped Maggiore Policlin, Neurol Unit, Via Francesco Sforza 35, I-20122 Milan, Italy论文数: 引用数: h-index:机构:Duga, Stefano论文数: 0 引用数: 0 h-index: 0机构: Humanitas Univ, Dept Biomed Sci, Milan, Italy Humanitas Clin & Res Ctr, Milan, Italy Fdn IRCCS Ca Granda Osped Maggiore Policlin, Neurol Unit, Via Francesco Sforza 35, I-20122 Milan, ItalyDi Fonzo, Alessio论文数: 0 引用数: 0 h-index: 0机构: Fdn IRCCS Ca Granda Osped Maggiore Policlin, Neurol Unit, Via Francesco Sforza 35, I-20122 Milan, Italy Univ Milan, Neurosci Sect, Dept Pathophysiol & Transplantat, Dino Ferrari Ctr, Milan, Italy Fdn IRCCS Ca Granda Osped Maggiore Policlin, Neurol Unit, Via Francesco Sforza 35, I-20122 Milan, Italy
- [46] A COL4A4 novel founder mutation causes autosomal recessive Alport syndrome in the Cypriot populationEUROPEAN JOURNAL OF HUMAN GENETICS, 2024, 32 : 1608 - 1608Polydorou, Christiana论文数: 0 引用数: 0 h-index: 0机构: Univ Cyprus, Biobankcy Ctr Excellence Biobanking & Biomed Res, Nicosia, Cyprus Univ Cyprus, Biobankcy Ctr Excellence Biobanking & Biomed Res, Nicosia, CyprusPapagregoriou, Gregory论文数: 0 引用数: 0 h-index: 0机构: Univ Cyprus, Biobankcy Ctr Excellence Biobanking & Biomed Res, Nicosia, Cyprus Univ Cyprus, Biobankcy Ctr Excellence Biobanking & Biomed Res, Nicosia, CyprusHadjipanagi, Despina论文数: 0 引用数: 0 h-index: 0机构: Univ Cyprus, Biobankcy Ctr Excellence Biobanking & Biomed Res, Nicosia, Cyprus Univ Cyprus, Biobankcy Ctr Excellence Biobanking & Biomed Res, Nicosia, CyprusMichael, George论文数: 0 引用数: 0 h-index: 0机构: Univ Cyprus, Biobankcy Ctr Excellence Biobanking & Biomed Res, Nicosia, Cyprus Univ Cyprus, Biobankcy Ctr Excellence Biobanking & Biomed Res, Nicosia, CyprusYioukkas, Lakis论文数: 0 引用数: 0 h-index: 0机构: Paphos Gen Hosp, Dept Nephrol, Paphos, Cyprus Univ Cyprus, Biobankcy Ctr Excellence Biobanking & Biomed Res, Nicosia, CyprusKkolou, Maria论文数: 0 引用数: 0 h-index: 0机构: Larnaca Gen Hosp, Dept Nephrol, Larnax, Cyprus Univ Cyprus, Biobankcy Ctr Excellence Biobanking & Biomed Res, Nicosia, CyprusPastelli, Androulla论文数: 0 引用数: 0 h-index: 0机构: Larnaca Gen Hosp, Dept Nephrol, Larnax, Cyprus Univ Cyprus, Biobankcy Ctr Excellence Biobanking & Biomed Res, Nicosia, CyprusLoukaidou, Panayiota论文数: 0 引用数: 0 h-index: 0机构: Larnaca Gen Hosp, Dept Nephrol, Larnax, Cyprus Univ Cyprus, Biobankcy Ctr Excellence Biobanking & Biomed Res, Nicosia, CyprusPipili, Chrysoula论文数: 0 引用数: 0 h-index: 0机构: Famagusta Gen Hosp, Dept Nephrol, Paralimni, Cyprus Univ Cyprus, Biobankcy Ctr Excellence Biobanking & Biomed Res, Nicosia, CyprusConstantinou, Kypros论文数: 0 引用数: 0 h-index: 0机构: Nicosia Gen Hosp, Transplant Ctr, Nicosia, Cyprus Univ Cyprus, Biobankcy Ctr Excellence Biobanking & Biomed Res, Nicosia, CyprusElpida, Toumasi论文数: 0 引用数: 0 h-index: 0机构: Nicosia Gen Hosp, Transplant Ctr, Nicosia, Cyprus Univ Cyprus, Biobankcy Ctr Excellence Biobanking & Biomed Res, Nicosia, CyprusSavva, Isavella论文数: 0 引用数: 0 h-index: 0机构: Nicosia Gen Hosp, Transplant Ctr, Nicosia, Cyprus Univ Cyprus, Biobankcy Ctr Excellence Biobanking & Biomed Res, Nicosia, CyprusSoloukides, Andreas论文数: 0 引用数: 0 h-index: 0机构: Nicosia Gen Hosp, Transplant Ctr, Nicosia, Cyprus Univ Cyprus, Biobankcy Ctr Excellence Biobanking & Biomed Res, Nicosia, CyprusDeltas, Constantinos论文数: 0 引用数: 0 h-index: 0机构: Univ Cyprus, Biobankcy Ctr Excellence Biobanking & Biomed Res, Nicosia, Cyprus Univ Cyprus, Univ Cyprus Med Sch, Nicosia, Cyprus Univ Cyprus, Biobankcy Ctr Excellence Biobanking & Biomed Res, Nicosia, Cyprus
- [47] Identification of a novel nonsense mutation in RP1 that causes autosomal recessive retinitis pigmentosa in an Indonesian familyMOLECULAR VISION, 2012, 18 (254-55): : 2411 - 2419Siemiatkowska, Anna M.论文数: 0 引用数: 0 h-index: 0机构: Radboud Univ Nijmegen, Med Ctr, Dept Human Genet, NL-6525 GA Nijmegen, Netherlands Radboud Univ Nijmegen, Med Ctr, Dept Human Genet, NL-6525 GA Nijmegen, NetherlandsAstuti, Galuh D. N.论文数: 0 引用数: 0 h-index: 0机构: Radboud Univ Nijmegen, Med Ctr, Dept Human Genet, NL-6525 GA Nijmegen, Netherlands Diponegoro Univ, Fac Med, Ctr Biomed Res, Div Human Genet, Semarang, Indonesia Radboud Univ Nijmegen, Med Ctr, Dept Human Genet, NL-6525 GA Nijmegen, NetherlandsArimadyo, Kentar论文数: 0 引用数: 0 h-index: 0机构: Diponegoro Univ, Fac Med, Ctr Biomed Res, Div Human Genet, Semarang, Indonesia Diponegoro Univ, Dr Kariadi Hosp, Fac Med, Dept Ophthalmol, Semarang, Indonesia Radboud Univ Nijmegen, Med Ctr, Dept Human Genet, NL-6525 GA Nijmegen, Netherlandsden Hollander, Anneke I.论文数: 0 引用数: 0 h-index: 0机构: Radboud Univ Nijmegen, Med Ctr, Dept Human Genet, NL-6525 GA Nijmegen, Netherlands Radboud Univ Nijmegen, Med Ctr, Dept Ophthalmol, NL-6525 GA Nijmegen, Netherlands Radboud Univ Nijmegen, Med Ctr, Dept Human Genet, NL-6525 GA Nijmegen, NetherlandsFaradz, Sultana M. H.论文数: 0 引用数: 0 h-index: 0机构: Diponegoro Univ, Fac Med, Ctr Biomed Res, Div Human Genet, Semarang, Indonesia Radboud Univ Nijmegen, Med Ctr, Dept Human Genet, NL-6525 GA Nijmegen, NetherlandsCremers, Frans P. M.论文数: 0 引用数: 0 h-index: 0机构: Radboud Univ Nijmegen, Med Ctr, Dept Human Genet, NL-6525 GA Nijmegen, Netherlands Radboud Univ Nijmegen, Med Ctr, Nijmegen Ctr Mol Life Sci, NL-6525 GA Nijmegen, Netherlands Radboud Univ Nijmegen, Med Ctr, Dept Human Genet, NL-6525 GA Nijmegen, NetherlandsCollin, Rob W. J.论文数: 0 引用数: 0 h-index: 0机构: Radboud Univ Nijmegen, Med Ctr, Dept Human Genet, NL-6525 GA Nijmegen, Netherlands Radboud Univ Nijmegen, Med Ctr, Nijmegen Ctr Mol Life Sci, NL-6525 GA Nijmegen, Netherlands Radboud Univ Nijmegen, Med Ctr, Dept Human Genet, NL-6525 GA Nijmegen, Netherlands
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