An ARG403GLN β-myosin heavy chain gene mutation identified in an Italian family with hypertrophic cardiomyopathy: description of clinical features of the family members

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Bibliographic Details
Published in:European heart journal 1997-06, Vol.18 (6), p.1033-1034
Main Authors: CONTE, M. R., MORELLO, M., MANGIARDI, L., ORZAN, F., CHECCO, L., BONFIGLIO, G., ALFARANO, A., CAMASCHELLA, C., BRUSCA, A.
Format: Article
Language:English
Subjects:
Adult
Cardiomyopathy, Hypertrophic - blood
Cardiomyopathy, Hypertrophic - diagnosis
Cardiomyopathy, Hypertrophic - genetics
Child
Child, Preschool
DNA - blood
DNA - genetics
Echocardiography
Electrocardiography
Female
Genetic Linkage
Humans
Italy
Male
Middle Aged
Mutation - genetics
Myosin Heavy Chains - genetics
Pedigree
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Summary:
ISSN:0195-668X
1522-9645
DOI:10.1093/oxfordjournals.eurheartj.a015364