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Chaperone therapy for Krabbe disease: potential for late-onset GALC mutations.
Hossain, Mohammad Arif; Higaki, Katsumi; Saito, Seiji; Ohno, Kazuki; Sakuraba, Hitoshi; Nanba, Eiji; Suzuki, Yoshiyuki; Ozono, Keiichi; Sakai, Norio.
Afiliação
  • Hossain MA; Department of Pediatrics, Osaka University Graduate School of Medicine, Osaka, Japan.
  • Higaki K; Division of Functional Genomics, Research Center for Bioscience and Technology, Tottori University, Yonago, Japan.
  • Saito S; Department of Medical Management and Informatics, Hokkaido Information University, Hokkaido, Japan.
  • Ohno K; NPO for the Promotion of Research on Intellectual Property Tokyo, Tokyo, Japan.
  • Sakuraba H; Department of Clinical Genetics, Meiji Pharmaceutical University, Tokyo, Japan.
  • Nanba E; Division of Functional Genomics, Research Center for Bioscience and Technology, Tottori University, Yonago, Japan.
  • Suzuki Y; Tokyo Metropolitan Institute of Medical Science, Tokyo, Japan.
  • Ozono K; Department of Pediatrics, Osaka University Graduate School of Medicine, Osaka, Japan.
  • Sakai N; Department of Pediatrics, Osaka University Graduate School of Medicine, Osaka, Japan.
J Hum Genet ; 60(9): 539-45, 2015 Sep.
Article em En | MEDLINE | ID: mdl-26108143

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Galactosilceramidase / Hexosaminas / Leucodistrofia de Células Globoides Idioma: En Revista: J Hum Genet Ano de publicação: 2015 Tipo de documento: Article País de afiliação: Japão

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Galactosilceramidase / Hexosaminas / Leucodistrofia de Células Globoides Idioma: En Revista: J Hum Genet Ano de publicação: 2015 Tipo de documento: Article País de afiliação: Japão