Molecular pathology of familial hypertrophic cardiomyopathy caused by mutations in the cardiac myosin binding protein C gene. | J Med Genet;35(3): 205-10, 1998 Mar. | MEDLINE

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Molecular pathology of familial hypertrophic cardiomyopathy caused by mutations in the cardiac myosin binding protein C gene.

Yu, B; French, J A; Carrier, L; Jeremy, R W; McTaggart, D R; Nicholson, M R; Hambly, B; Semsarian, C; Richmond, D R; Schwartz, K; Trent, R J.

Affiliation

Yu B; Department of Molecular and Clinical Genetics, Royal Prince Alfred Hospital, Sydney, NSW, Australia.

J Med Genet ; 35(3): 205-10, 1998 Mar.

Article in En | MEDLINE | ID: mdl-9541104

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cardiomyopathy, Hypertrophic / Carrier Proteins / Myosins Limits: Female / Humans / Male / Middle aged Country/Region as subject: Oceania Language: En Journal: J Med Genet Year: 1998 Document type: Article Affiliation country:

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cardiomyopathy, Hypertrophic / Carrier Proteins / Myosins Limits: Female / Humans / Male / Middle aged Country/Region as subject: Oceania Language: En Journal: J Med Genet Year: 1998 Document type: Article Affiliation country: