Mapping of a novel gene for familial hypertrophic cardiomyopathy to chromosome 11
Carrier, L. ; Hengstenberg, C. ; Beckmann, J. S. ; Guicheney, P. ; Dufour, C. ; Bercovici, J. ; Dausse, E. ; Berebbi-Bertrand, I. ; Wisnewsky, C. ; Pulvenis, D. ; Fetler, L. ; Vignal, A. ; Weissenbach, J. ; Hillaire, D. ; Feingold, J. ; Bouhour, J.-B. ; Hagege, A. ; Desnos, M. ; Isnard, R. ; Dubourg, O. ; Komajda, M. ; Schwartz, K.
[s.l.] : Nature Publishing Group
Published 1993
[s.l.] : Nature Publishing Group
Published 1993
| ISSN: |
1546-1718
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|---|---|
| Source: |
Nature Archives 1869 - 2009
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| Topics: |
Biology
Medicine
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| Notes: |
[Auszug] Familial hypertrophic cardiomyopathy (FHC) is a cardiac disorder transmitted as an autosomal dominant trait. FHC has been shown to be genetically heterogeneous with less than 50% of published pedigrees being associated with mutations in the p myosin heavy chain (β–MHC) gene on chromosome ...
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| Type of Medium: |
Electronic Resource
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| URL: |