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Dihydropyridine Receptor Congenital Myopathy In A Consangineous Turkish Family.
Yis, Uluç; Hiz, Semra; Günes, Sezgin; Diniz, Gülden; Baydan, Figen; Töpf, Ana; Sonmezler, Ece; Lochmüller, Hanns; Horvath, Rita; Oktay, Yavuz.
Afiliação
  • Yis U; Department of Pediatrics, Dokuz Eylül University, School of Medicine, Division of Child Neurology, Izmir, Turkey.
  • Hiz S; Department of Pediatrics, Dokuz Eylül University, School of Medicine, Division of Child Neurology, Izmir, Turkey.
  • Günes S; Department of Neonatology, Medical Park Hospital, Izmir, Turkey.
  • Diniz G; Tepecik Research and Training Hospital, University of Health Sciences, Izmir, Turkey.
  • Baydan F; Tepecik Research and Training Hospital, University of Health Sciences, Izmir, Turkey.
  • Töpf A; John Walton Muscular Dystrophy Research Centre, Institute of Genetic Medicine, Newcastle University, Newcastle upon Tyne, UK.
  • Sonmezler E; Izmir International Biomedicine and Genom Institute, Dokuz Eylul University, Izmir, Turkey.
  • Lochmüller H; Department of Medicine, Children's Hospital of Eastern Ontario Research Institute, University of Ottawa, Ottawa, Canada and Division of Neurology, The Ottawa Hospital, Ottawa, Canada.
  • Horvath R; Department of Clinical Neurosciences, University of Cambridge School of Clinical, Medicine, Cambridge Biomedical Campus, Cambridge, UK.
  • Oktay Y; Izmir International Biomedicine and Genom Institute, Dokuz Eylul University, Izmir, Turkey.
J Neuromuscul Dis ; 6(3): 377-384, 2019.
Article em En | MEDLINE | ID: mdl-31227654

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Canais de Cálcio Tipo L / Miotonia Congênita Limite: Child, preschool / Female / Humans / Infant / Male País/Região como assunto: Asia Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Canais de Cálcio Tipo L / Miotonia Congênita Limite: Child, preschool / Female / Humans / Infant / Male País/Região como assunto: Asia Idioma: En Ano de publicação: 2019 Tipo de documento: Article