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Charcot-Marie-Tooth disease type 2 and P0 gene mutations.
Pareyson, D; Sghirlanzoni, A; Bolti, S; Ciano, C; Fallica, E; Mora, M; Taroni, F.
Neurology ; 52(5): 1110-1, 1999 Mar 23.
Article in En | MEDLINE | ID: mdl-10102454
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Collection: 01-internacional Database: MEDLINE Main subject: Charcot-Marie-Tooth Disease / Myelin P0 Protein Limits: Adult / Female / Humans Language: En Journal: Neurology Year: 1999 Document type: Article Country of publication:
Search on Google
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PubMed Links

Collection: 01-internacional Database: MEDLINE Main subject: Charcot-Marie-Tooth Disease / Myelin P0 Protein Limits: Adult / Female / Humans Language: En Journal: Neurology Year: 1999 Document type: Article Country of publication: