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X-linked dilated cardiomyopathy. Molecular genetic evidence of linkage to the Duchenne muscular dystrophy (dystrophin) gene at the Xp21 locus.
J A JA Towbin, J F JF Hejtmancik, P P Brink, B B Gelb, X M XM Zhu, J S JS Chamberlain, E R ER McCabe and M M Swift
Circulation 87(6):1854-65 (1993)
PMID 8504498
X-linked cardiomyopathy (XLCM) is a rapidly progressive primary myocardial disorder presenting in teenage males as congestive heart failure. Manifesting female carriers have later onset (fifth decade) and slower progression. The purpose of this study was to localize the XLCM gene locus in two families using molecular genetic techniques.
DOI:
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DOI:
Version: za2963e q8zad q8zbc q8zc3 q8zd7 q8ze2 q8zf6 q8zg1