Charcot-Marie-Tooth disease type 2 and P0 gene mutations.

Neurology ·Vol. 52 ·No. 5 ·1999-03-23 ·Pages 1110-1

Pareyson D, Sghirlanzoni A, Bolti S, Ciano C, Fallica E, Mora M, Taroni F

Abstract

暂无摘要

MeSH Terms

Adult Charcot-Marie-Tooth Disease/genetics Female Humans Mutation Myelin P0 Protein/genetics Phenotype

Chemicals

Myelin P0 Protein

Authors & Affiliations

7 authors, click to expand affiliations / ORCID

Pareyson D

Sghirlanzoni A

Bolti S

Ciano C

Fallica E

Mora M

Taroni F

Article Info

Journal

Neurology

Abbr.

Neurology

ISSN

0028-3878

DOI

Published

1999-03-23

Pages

1110-1

Language

English

Region

United States

NLM ID

0401060

Subset

Grants

Telethon · 924 · Italy

Corrections

CommentOn

PMID: 9595994

External Links

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