Your browser doesn't support javascript.
loading
A novel lamin A/C gene mutation causing spinal muscular atrophy phenotype with cardiac involvement: report of one case.
Iwahara, Naotoshi; Hisahara, Shin; Hayashi, Takashi; Kawamata, Jun; Shimohama, Shun.
Afiliação
  • Iwahara N; Department of Neurology, School of Medicine, Sapporo Medical University, South 1 West 16, Chuo-ku, Sapporo, 060-8543, Japan. n.iwahara@sapmed.ac.jp.
  • Hisahara S; Department of Neurology, School of Medicine, Sapporo Medical University, South 1 West 16, Chuo-ku, Sapporo, 060-8543, Japan. hisahara@sapmed.ac.jp.
  • Hayashi T; Department of Neurology, School of Medicine, Sapporo Medical University, South 1 West 16, Chuo-ku, Sapporo, 060-8543, Japan. takashi@sapmed.ac.jp.
  • Kawamata J; Department of Pharmacology, School of Medicine, Sapporo Medical University, South 1 West 16, Chuo-ku, Sapporo, 060-8543, Japan. takashi@sapmed.ac.jp.
  • Shimohama S; Department of Neurology, School of Medicine, Sapporo Medical University, South 1 West 16, Chuo-ku, Sapporo, 060-8543, Japan. jkawamata@sapmed.ac.jp.
BMC Neurol ; 15: 13, 2015 Feb 20.
Article em En | MEDLINE | ID: mdl-25886484

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Limite: Aged / Humans / Male Idioma: En Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Limite: Aged / Humans / Male Idioma: En Ano de publicação: 2015 Tipo de documento: Article