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Familial hypertrophic cardiomyopathy is a genetically heterogeneous disease.
We demonstrate that familial hypertrophic cardiomyopathy (FHC), an autosomal dominant disorder of heart muscle, is a genetically heterogeneous disease. The locus responsible for FHC in members of one large kindred was recently mapped to chromosome 14q11-12 (FHC-1). We have characterized three additi...
Tallennettuna:
| Julkaisussa: | J Clin Invest |
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| Päätekijät: | , , , , , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
American Society for Clinical Investigation
1990
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC296820/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/1975599/ https://ncbi.nlm.nih.govhttps://doi.org/10.1172/JCI114802 |
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