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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
9217
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pubmed:dateCreated |
2000-6-27
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pubmed:abstractText |
In a systematic analysis of inherited forms of cardiomyopathy, we previously identified a family with X-linked dilated cardiomyopathy characterised by a mutation in the rod region of dystrophin. We have now attempted to eludicate the genetic mechanism involved in this disease, as well as the role of dystrophin-associated glycoproteins.
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
AIM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:month |
May
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pubmed:issn |
0140-6736
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pubmed:author |
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pubmed:issnType |
Print
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pubmed:day |
20
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pubmed:volume |
355
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1781-5
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pubmed:dateRevised |
2010-11-18
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pubmed:meshHeading |
pubmed-meshheading:10832829-Cardiomyopathy, Dilated,
pubmed-meshheading:10832829-Codon, Nonsense,
pubmed-meshheading:10832829-Cytoskeletal Proteins,
pubmed-meshheading:10832829-Dystroglycans,
pubmed-meshheading:10832829-Dystrophin,
pubmed-meshheading:10832829-Female,
pubmed-meshheading:10832829-Genetic Linkage,
pubmed-meshheading:10832829-Humans,
pubmed-meshheading:10832829-Male,
pubmed-meshheading:10832829-Membrane Glycoproteins,
pubmed-meshheading:10832829-Mutation,
pubmed-meshheading:10832829-Pedigree,
pubmed-meshheading:10832829-Sarcoglycans,
pubmed-meshheading:10832829-X Chromosome
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pubmed:year |
2000
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pubmed:articleTitle |
Association of nonsense mutation of dystrophin gene with disruption of sarcoglycan complex in X-linked dilated cardiomyopathy.
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pubmed:affiliation |
Medizinische Klinik II, University of Lübeck, Germany. franz@medinf.mu-luebeck.de
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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