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Frequency of de novo mutations in Japanese patients with Fabry disease.
Kobayashi, Masahisa; Ohashi, Toya; Iizuka, Sayoko; Kaneshiro, Eiko; Higuchi, Takashi; Eto, Yoshikatsu; Ida, Hiroyuki.
Afiliación
  • Kobayashi M; Department of Pediatrics, The Jikei University School of Medicine, Tokyo, Japan.
  • Ohashi T; Department of Pediatrics, The Jikei University School of Medicine, Tokyo, Japan; Division of Gene Therapy, Research Center for Medical Sciences, The Jikei University School of Medicine, Tokyo, Japan.
  • Iizuka S; Division of Gene Therapy, Research Center for Medical Sciences, The Jikei University School of Medicine, Tokyo, Japan.
  • Kaneshiro E; Department of Pediatrics, The Jikei University School of Medicine, Tokyo, Japan.
  • Higuchi T; Division of Gene Therapy, Research Center for Medical Sciences, The Jikei University School of Medicine, Tokyo, Japan.
  • Eto Y; Advanced Clinical Research Center, Institute of Neurological Disorders, Kanagawa, Japan.
  • Ida H; Department of Pediatrics, The Jikei University School of Medicine, Tokyo, Japan; Division of Gene Therapy, Research Center for Medical Sciences, The Jikei University School of Medicine, Tokyo, Japan.
Mol Genet Metab Rep ; 1: 283-287, 2014.
Article en En | MEDLINE | ID: mdl-27896102
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Mol Genet Metab Rep Año: 2014 Tipo del documento: Article País de afiliación: Japón Pais de publicación: Estados Unidos
Texto completo
Añadir a Mi BVS
Imprimir
XML
PubMed Links
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Mol Genet Metab Rep Año: 2014 Tipo del documento: Article País de afiliación: Japón Pais de publicación: Estados Unidos