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Genetic linkage of a novel autosomal dominant restrictive cardiomyopathy locus
Background: In recent years, non-syndromic idiopathic cardiomyopathies have increasingly been characterised as autosomal dominant conditions caused by single gene mutations. Loci have been identified for hypertrophic and dilated cardiomyopathy, and in some cases the same loci are associated with res...
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| Hlavní autoři: | , , , , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
BMJ Group
2005
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1736124/ https://ncbi.nlm.nih.gov/pubmed/16061566 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jmg.2004.030189 |
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