Home LiteratureArticle Details
PMID: 12499472 Published · ppublish English Comment Editorial

GDAP1 mutations in CMT4: axonal and demyelinating phenotypes?: The exception "proves the rule".

Neurology ·Vol. 59 ·No. 12 ·2002-12-24 ·Pages 1835-6

Nicholson G, Ouvrier R

Abstract

暂无摘要

MeSH Terms
Axons/pathology Charcot-Marie-Tooth Disease/genetics,pathology Demyelinating Diseases/genetics,pathology Genes, Recessive/genetics Humans Nerve Tissue Proteins/genetics Phenotype
Chemicals
GDAP protein Nerve Tissue Proteins
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Nicholson Garth
Ouvrier Robert
Article Info
Journal
Neurology
Abbr.
Neurology
ISSN
0028-3878
DOI
10.1212/wnl.59.12.1835
Published
2002-12-24
Pages
1835-6
Language
English
Region
United States
NLM ID
0401060
Subset
IM
Corrections
CommentOn
PMID: 12499475
External Links
PubMed source DOI: 10.1212/wnl.59.12.1835 View journal details
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