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Corrigendum to "A homozygous DPM3 mutation in a patient with alpha-dystroglycan-related limb girdle muscular dystrophy" [Neuromuscular disorders 27/11 (2017) 1043-1046].
Van den Bergh, P Y K; Sznajer, Y; Van Parys, V; van Tol, W; Wevers, R A; Lefeber, D J; Xu, L; Lek, M; MacArthur, D G; Johnson, K; Phillips, L; Töpf, A; Straub, V.
Afiliação
  • Van den Bergh PYK; Neuromuscular Reference Centre, University Hospital St-Luc, University of Louvain, Brussels, Belgium. Electronic address: peter.vandenbergh@uclouvain.be.
  • Sznajer Y; Neuromuscular Reference Centre, University Hospital St-Luc, University of Louvain, Brussels, Belgium; Centre for Human Genetics, University Hospital St-Luc, University of Louvain, Brussels, Belgium.
  • Van Parys V; Neuromuscular Reference Centre, University Hospital St-Luc, University of Louvain, Brussels, Belgium.
  • van Tol W; Department of Neurology, Radboud University Medical Centre, Nijmegen, The Netherlands; Translational Metabolic Laboratory, Radboud University Medical Centre, Nijmegen, The Netherlands.
  • Wevers RA; Translational Metabolic Laboratory, Radboud University Medical Centre, Nijmegen, The Netherlands.
  • Lefeber DJ; Department of Neurology, Radboud University Medical Centre, Nijmegen, The Netherlands; Translational Metabolic Laboratory, Radboud University Medical Centre, Nijmegen, The Netherlands.
  • Xu L; Analytic and Translational Genetics Unit, Massachusetts General Hospital, Boston, MA 02114, USA; Program in Medical and Population Genetics, Broad Institute of Harvard and MIT, Cambridge, MA 02142, USA.
  • Lek M; Analytic and Translational Genetics Unit, Massachusetts General Hospital, Boston, MA 02114, USA; Program in Medical and Population Genetics, Broad Institute of Harvard and MIT, Cambridge, MA 02142, USA.
  • MacArthur DG; Analytic and Translational Genetics Unit, Massachusetts General Hospital, Boston, MA 02114, USA; Program in Medical and Population Genetics, Broad Institute of Harvard and MIT, Cambridge, MA 02142, USA.
  • Johnson K; The John Walton Muscular Dystrophy Research Centre, Institute of Genetic Medicine, Newcastle University, Newcastle upon Tyne, United Kingdom.
  • Phillips L; The John Walton Muscular Dystrophy Research Centre, Institute of Genetic Medicine, Newcastle University, Newcastle upon Tyne, United Kingdom.
  • Töpf A; The John Walton Muscular Dystrophy Research Centre, Institute of Genetic Medicine, Newcastle University, Newcastle upon Tyne, United Kingdom.
  • Straub V; The John Walton Muscular Dystrophy Research Centre, Institute of Genetic Medicine, Newcastle University, Newcastle upon Tyne, United Kingdom.
Neuromuscul Disord ; 28(1): 101, 2018 01.
Article em En | MEDLINE | ID: mdl-29246662
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Neuromuscul Disord Ano de publicação: 2018 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Neuromuscul Disord Ano de publicação: 2018 Tipo de documento: Article