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Variation p.R1045H in MYH7 correlated with hypertrophic cardiomyopathy in a Chinese pedigree
BACKGROUND: Inherited hypertrophic cardiomyopathy (HCM) is a common heart muscle disease that damages heart function and may cause the heart to suddenly stop beating. Genetic factors play an important role in HCM. Pedigree analysis is a good way to identify the genetic defects that cause disease. ME...
Kaydedildi:
| Yayımlandı: | BMC Med Genomics |
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| Asıl Yazarlar: | , , , , , , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
BioMed Central
2021
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8325323/ https://ncbi.nlm.nih.gov/pubmed/34330286 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12920-021-01046-2 |
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