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机译:西班牙先天性染发素综合征的分子表征
Department of Neuromuscular Diseases Hospital Sant Joan de Déu;
John Walton Muscular Dystrophy Research Centre MRC Centre for Neuromuscular Diseases Institute of;
Department of Neurology Hospital Universitari La Fe Universitat de Valencia;
Department of Genetics Hospital de la Santa Creu i Sant Pau and CIBERER U705;
Department of Pediatrics Hospital Universitario Marqués de Valdecilla;
Neuromuscular Diseases Unit Department of Neurology Hospital de la Santa Creu i Sant Pau;
Department of Neuromuscular Diseases Hospital Sant Joan de Déu;
Department of Neurology Hospital General San Jorge;
Department of Genetics Hospital de la Santa Creu i Sant Pau and CIBERER U705;
Friedrich-Baur-Institute Ludwig-Maximilians-University Munich;
Friedrich-Baur-Institute Ludwig-Maximilians-University Munich;
Wellcome Trust Centre for Mitochondrial Research Institute of Genetic Medicine Newcastle;
Friedrich-Baur-Institute Ludwig-Maximilians-University Munich;
Department of Pediatrics Hospital Universitario Cruces;
Department of Neurology Hospital Universitari La Fe Universitat de Valencia;
John Walton Muscular Dystrophy Research Centre MRC Centre for Neuromuscular Diseases Institute of;
John Walton Muscular Dystrophy Research Centre MRC Centre for Neuromuscular Diseases Institute of;
John Walton Muscular Dystrophy Research Centre MRC Centre for Neuromuscular Diseases Institute of;
Neuropathology Unit Department of Pathology and Neuromuscular Unit IDIBELL-Hospital Universitari;
Neurosciences Group Nuffield Department of Clinical Neurosciences Weatherall Institute of;
Department of Pediatric Neurology Hospital Universitario 12 de Octubre;
Department of Pediatrics Hospital Universitario Rey Juan Carlos;
Department of Neuropediatrics Hospital General Universitario Gregorio Mara?ón;
Department of Neuropediatrics Complejo Hospitalario Universitario Insular Materno-Infantil;
Department of Neuropediatrics Hospital Virgen de la Salud;
Neuropathology Unit Department of Pathology and Neuromuscular Unit IDIBELL-Hospital Universitari;
Neuropathology Unit Department of Pathology and Neuromuscular Unit IDIBELL-Hospital Universitari;
Department of Neuromuscular Diseases Hospital Sant Joan de Déu;
Neurosciences Group Nuffield Department of Clinical Neurosciences Weatherall Institute of;
John Walton Muscular Dystrophy Research Centre MRC Centre for Neuromuscular Diseases Institute of;
Department of Neuromuscular Diseases Hospital Sant Joan de Déu;
Congenital myasthenic syndrome; Genetic mutations; CHRNE; RAPSN; GFPT1; COLQ; DOK7; GMPPB; Slow-channel syndrome;
机译:西班牙先天性染发素综合征的分子表征
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机译:先天性肌腱综合征的新视野
机译:对Peters Plus综合征和先天性障碍的分子机制调查重叠表型
机译:有或没有促进的突触前先天性肌无力综合征的电生理:从电诊断结果到分子机制。
机译:先天性染发素综合征 - 神经肌肉交配蛋白质缺陷的分子基