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Muscular dystrophy and neuronal migration disorder caused by mutations in a glycosyltransferase, POMGnT1.
Yoshida, A; Kobayashi, K; Manya, H; Taniguchi, K; Kano, H; Mizuno, M; Inazu, T; Mitsuhashi, H; Takahashi, S; Takeuchi, M; Herrmann, R; Straub, V; Talim, B; Voit, T; Topaloglu, H; Toda, T; Endo, T.
Affiliation
  • Yoshida A; Central Laboratories for Key Technology, Kirin Brewery Co., Ltd., Kanazawa-ku, 236-0004, Yokohama, Japan.
Dev Cell ; 1(5): 717-24, 2001 Nov.
Article in En | MEDLINE | ID: mdl-11709191
Subject(s)
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Collection: 01-internacional Database: MEDLINE Main subject: Cell Movement / Glycosyltransferases / Point Mutation / N-Acetylglucosaminyltransferases / Muscular Dystrophies Type of study: Prognostic_studies Limits: Child, preschool / Female / Humans / Male Language: En Journal: Dev Cell Journal subject: EMBRIOLOGIA Year: 2001 Document type: Article Affiliation country: Japón Country of publication: Estados Unidos
Search on Google
Add to My VHL
Print
XML
PubMed Links

Collection: 01-internacional Database: MEDLINE Main subject: Cell Movement / Glycosyltransferases / Point Mutation / N-Acetylglucosaminyltransferases / Muscular Dystrophies Type of study: Prognostic_studies Limits: Child, preschool / Female / Humans / Male Language: En Journal: Dev Cell Journal subject: EMBRIOLOGIA Year: 2001 Document type: Article Affiliation country: Japón Country of publication: Estados Unidos