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Autosomal recessive limb-girdle and Miyoshi muscular dystrophies in the Netherlands: The clinical and molecular spectrum of 244 patients.
Ten Dam, Leroy; Frankhuizen, Wendy S; Linssen, Wim H J P; Straathof, Chiara S; Niks, Erik H; Faber, Karin; Fock, Annemarie; Kuks, Jan B; Brusse, Esther; de Coo, René; Voermans, Nicol; Verrips, Aad; Hoogendijk, Jessica E; van der Pol, Ludo; Westra, Dineke; de Visser, Marianne; van der Kooi, Anneke J; Ginjaar, Ieke.
Afiliação
  • Ten Dam L; Department of Neurology, Amsterdam University Medical Centre, Amsterdam Neuroscience, Amsterdam, The Netherlands.
  • Frankhuizen WS; Department of Clinical Genetics, Leiden University Medical Centre, Leiden, The Netherlands.
  • Linssen WHJP; Department of Neurology, OLVG-West Hospital, Amsterdam, The Netherlands.
  • Straathof CS; Department of Neurology, Leiden University Medical Centre, Leiden, The Netherlands.
  • Niks EH; Department of Neurology, Leiden University Medical Centre, Leiden, The Netherlands.
  • Faber K; Department of Neurology, Maastricht University Medical Centre, Maastricht, The Netherlands.
  • Fock A; Department of Neurology, University Medical Centre Groningen, Groningen, The Netherlands.
  • Kuks JB; Department of Neurology, University Medical Centre Groningen, Groningen, The Netherlands.
  • Brusse E; Department of Neurology, Erasmus MC University Medical Centre, Rotterdam, The Netherlands.
  • de Coo R; Department of Neurology, Erasmus MC University Medical Centre, Rotterdam, The Netherlands.
  • Voermans N; Department of Neurology, Radboud University Medical Centre, Nijmegen, The Netherlands.
  • Verrips A; Department of Neurology, Canisius Wilhelmina Hospital Nijmegen, Nijmegen, The Netherlands.
  • Hoogendijk JE; Department of Neurology, Rudolf Magnus Institute of Neuroscience, University Medical Center, Utrecht, The Netherlands.
  • van der Pol L; Department of Neurology, Rudolf Magnus Institute of Neuroscience, University Medical Center, Utrecht, The Netherlands.
  • Westra D; Department of Human Genetics, Radboud University Medical Centre, Nijmegen, The Netherlands.
  • de Visser M; Department of Neurology, Amsterdam University Medical Centre, Amsterdam Neuroscience, Amsterdam, The Netherlands.
  • van der Kooi AJ; Department of Neurology, Amsterdam University Medical Centre, Amsterdam Neuroscience, Amsterdam, The Netherlands.
  • Ginjaar I; Department of Clinical Genetics, Leiden University Medical Centre, Leiden, The Netherlands.
Clin Genet ; 96(2): 126-133, 2019 08.
Article em En | MEDLINE | ID: mdl-30919934
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Predisposição Genética para Doença / Distrofia Muscular do Cíngulo dos Membros Tipo de estudo: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies / Screening_studies Limite: Female / Humans / Male País como assunto: Europa Idioma: En Ano de publicação: 2019 Tipo de documento: Article
Texto completo
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Predisposição Genética para Doença / Distrofia Muscular do Cíngulo dos Membros Tipo de estudo: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies / Screening_studies Limite: Female / Humans / Male País como assunto: Europa Idioma: En Ano de publicação: 2019 Tipo de documento: Article