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Mutations in the human δ-sarcoglycan gene in familial and sporadic dilated cardiomyopathy

Dilated cardiomyopathy (DCM) is a major cause of morbidity and mortality. Two genes have been identified for the X-linked forms (dystrophin and tafazzin), whereas three other genes (actin, lamin A/C, and desmin) cause autosomal dominant DCM; seven other loci for autosomal dominant DCM have been mapp...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Prif Awduron: Tsubata, Shinichi, Bowles, Karla R., Vatta, Matteo, Zintz, Carmelann, Titus, Jack, Muhonen, Linda, Bowles, Neil E., Towbin, Jeffrey A.
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: American Society for Clinical Investigation 2000
Pynciau:
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC381284/
https://ncbi.nlm.nih.gov/pubmed/10974018
Tagiau: Ychwanegu Tag
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