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PMID: 9146999 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Review

Muscular dystrophies and the dystrophin-glycoprotein complex.

Current opinion in neurology ·Vol. 10 ·No. 2 ·1997-04-00 ·Pages 168-75

Straub V, Campbell KP

Abstract

Efforts to understand the function of dystrophin, the protein product for the Duchenne muscular dystrophy gene, resulted in the purification of the dystrophin-glycoprotein complex. Over the past year several novel components of this complex have been identified. Recent studies have extended the number of muscular dystrophies associated with the oligomeric complex to six genetically distinct diseases, including three new forms of limb-girdle muscular dystrophy and one form of congenital muscular dystrophy.

MeSH Terms
Animals Child Dystrophin/genetics,physiology Gene Expression/physiology Genotype Humans Membrane Glycoproteins/genetics,physiology Mice Mice, Transgenic Muscular Dystrophies/classification,genetics,physiopathology Phenotype
Chemicals
Dystrophin Membrane Glycoproteins
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Straub V
Howard Hughes Medical Institute, Department of Physiology and Biophysics, University of Iowa College of Medicine, Iowa City 52242, USA.
Campbell K P
Article Info
Journal
Current opinion in neurology
Abbr.
Curr Opin Neurol
ISSN
1350-7540
Published
1997-04-00
Pages
168-75
Language
English
Region
England
NLM ID
9319162
Subset
IM
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