Hereditary demyelinating neuropathy of infancy: a genetically complex syndrome.

Brain : a journal of neurology ·Vol. 120 ( Pt 11) ·1997-11-00 ·Pages 2113-5

Gambardella A, Muglia M, Quattrone A

Abstract

暂无摘要

MeSH Terms

Charcot-Marie-Tooth Disease/classification,genetics Demyelinating Diseases/classification,genetics Genetic Diseases, Inborn/classification,genetics Genetic Linkage Humans Infant

Authors & Affiliations

3 authors, click to expand affiliations / ORCID

Gambardella A

Muglia M

Quattrone A

Article Info

Journal

Brain : a journal of neurology

Abbr.

Brain

ISSN

0006-8950

DOI

10.1093/brain/120.11.2113

Published

1997-11-00

Pages

2113-5

Language

English

Region

England

NLM ID

0372537

Subset

Corrections

CommentOn

PMID: 9055797

External Links

PubMed source DOI: 10.1093/brain/120.11.2113 View journal details

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Hereditary demyelinating neuropathy of infancy: a genetically complex syndrome.

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