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PMID: 6583703 Published · ppublish English Journal Article

X chromosome-linked muscular dystrophy (mdx) in the mouse.

Bulfield G, Siller WG, Wight PA, Moore KJ

Abstract

An X chromosome-linked mouse mutant (gene symbol, mdx) has been found that has elevated plasma levels of muscle creatine kinase and pyruvate kinase and exhibits histological lesions characteristic of muscular dystrophy. The mutants show mild clinical symptoms and are viable and fertile. Linkage analysis with four X chromosome loci indicates that mdx maps in the Hq Bpa region of the mouse X chromosome. This gives a gene order of mdx-Tfm-Pgk-1-Ags, the same as for the equivalent genes on the human X chromosome.

MeSH Terms
Animals Crosses, Genetic Female Genetic Linkage Male Mice Mice, Inbred C57BL Mice, Mutant Strains Muscles/enzymology Muscular Dystrophy, Animal/enzymology,genetics,pathology Mutation Pyruvate Kinase/genetics,metabolism X Chromosome
Chemicals
Pyruvate Kinase
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Bulfield G
Siller W G
Wight P A
Moore K J
References (17)
17 references, click to expand
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Article Info
Journal
Proceedings of the National Academy of Sciences of the United States of America
Abbr.
Proc Natl Acad Sci U S A
ISSN
0027-8424
Published
1984-02-00
Pages
1189-92
Language
English
Region
United States
NLM ID
7505876
PMCID
PMC344791
Subset
IM
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