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Estimate of the abundance of cardiomyopathic mutations in the β-myosin gene
The steady discovery of new β-myosin mutations causing familial hypertrophic cardiomyopathy (FHCM) suggests that only a fraction of the total number of mutations has been identified so far by clinical screenings. To test this hypothesis, data derived from seven independent genetic studies were re-an...
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| Autori principali: | , , , |
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| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
2009
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2982777/ https://ncbi.nlm.nih.gov/pubmed/19174318 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ijcard.2008.12.199 |
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