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Penetrance of Hypertrophic Cardiomyopathy in Sarcomere Protein Mutation Carriers
BACKGROUND: Predictive genetic screening of relatives of patients with hypertrophic cardiomyopathy (HCM) caused by sarcomere protein (SP) gene mutations is current standard of care, but there are few data on long-term outcomes in mutation carriers without HCM. OBJECTIVES: The aim of this study was t...
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| Vydáno v: | J Am Coll Cardiol |
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| Hlavní autoři: | , , , , , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Elsevier Biomedical
2020
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7397507/ https://ncbi.nlm.nih.gov/pubmed/32731933 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.jacc.2020.06.011 |
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