Myosin mutations in hypertrophic cardiomyopathy and functional implications.

Vosberg, H P

Vosberg, H P.

Affiliation

Vosberg HP; Max-Planck-Institut für physiologische und klinische Forschung, Abteilung Experimentielle Kardiologie, Bad Nauheim.

Herz ; 19(2): 75-83, 1994 Apr.

Article in En | MEDLINE | ID: mdl-8194835

Subject(s)

Cardiomyopathy, Hypertrophic/genetics; Mutation/genetics; Myosins/genetics; Base Sequence/genetics; Calmodulin-Binding Proteins/genetics; Cardiomyopathy, Hypertrophic/physiopathology; Chromosomes, Human, Pair 14; DNA/genetics; Humans; Molecular Sequence Data; Myosin Heavy Chains; Myosin Type I; Myosins/physiology

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PubMed Links

Collection: 01-internacional Database: MEDLINE Main subject: Cardiomyopathy, Hypertrophic / Myosins / Mutation Limits: Humans Language: En Journal: Herz Year: 1994 Type: Article

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