Your browser doesn't support javascript.
loading
Genotype-phenotype correlations and effect of mutation location in Japanese CADASIL patients.
Mukai, Mao; Mizuta, Ikuko; Watanabe-Hosomi, Akiko; Koizumi, Takashi; Matsuura, Jun; Hamano, Ai; Tomimoto, Hidekazu; Mizuno, Toshiki.
Afiliação
  • Mukai M; Department of Neurology, Graduate School of Medical Science, Kyoto Prefectural University of Medicine, Kyoto, Japan.
  • Mizuta I; Department of Neurology, Graduate School of Medical Science, Kyoto Prefectural University of Medicine, Kyoto, Japan.
  • Watanabe-Hosomi A; Department of Neurology, Graduate School of Medical Science, Kyoto Prefectural University of Medicine, Kyoto, Japan.
  • Koizumi T; Department of Neurology, Graduate School of Medical Science, Kyoto Prefectural University of Medicine, Kyoto, Japan.
  • Matsuura J; Department of Neurology, Graduate School of Medical Science, Kyoto Prefectural University of Medicine, Kyoto, Japan.
  • Hamano A; Department of Neurology, Graduate School of Medical Science, Kyoto Prefectural University of Medicine, Kyoto, Japan.
  • Tomimoto H; Department of Neurology, Mie University Graduate School of Medicine, Tsu, Japan.
  • Mizuno T; Department of Neurology, Graduate School of Medical Science, Kyoto Prefectural University of Medicine, Kyoto, Japan. mizuno@koto.kpu-m.ac.jp.
J Hum Genet ; 65(8): 637-646, 2020 Aug.
Article em En | MEDLINE | ID: mdl-32277177

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: CADASIL / Receptor Notch3 Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Aged / Female / Humans / Male / Middle aged País/Região como assunto: Asia Idioma: En Revista: J Hum Genet Assunto da revista: GENETICA MEDICA Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Japão

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: CADASIL / Receptor Notch3 Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Aged / Female / Humans / Male / Middle aged País/Região como assunto: Asia Idioma: En Revista: J Hum Genet Assunto da revista: GENETICA MEDICA Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Japão