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PMID: 8829637 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Novel mutations in the connexin 32 gene associated with X-linked Charcot-Marie tooth disease.

Human mutation ·Vol. 7 ·No. 2 ·1996-00-00 ·Pages 167-71

Tan CC, Ainsworth PJ, Hahn AF, MacLeod PM

Abstract

暂无摘要

MeSH Terms
Base Sequence Canada Charcot-Marie-Tooth Disease/genetics,metabolism Connexins/chemistry,genetics DNA Primers/chemistry Female Genetic Linkage Humans Male Molecular Sequence Data Pedigree Point Mutation Polymerase Chain Reaction Polymorphism, Restriction Fragment Length X Chromosome
Chemicals
Connexins DNA Primers connexin 32
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Tan C C
Department of Medical Biochemistry, University of Western Ontario, Victoria Hospital, London, Canada.
Ainsworth P J
Hahn A F
MacLeod P M
Article Info
Journal
Human mutation
Abbr.
Hum Mutat
ISSN
1059-7794
Published
1996-00-00
Pages
167-71
Language
English
Region
United States
NLM ID
9215429
Subset
IM
Databases
GENBANK
X04325
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