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FBXO32, encoding a member of the SCF complex, is mutated in dilated cardiomyopathy
BACKGROUND: Dilated cardiomyopathy (DCM) is a common form of cardiomyopathy causing systolic dysfunction and heart failure. Rare variants in more than 30 genes, mostly encoding sarcomeric proteins and proteins of the cytoskeleton, have been implicated in familial DCM to date. Yet, the majority of va...
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| Опубликовано в: : | Genome Biol |
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| Главные авторы: | , , , , , , , , , , |
| Формат: | Artigo |
| Язык: | Inglês |
| Опубликовано: |
BioMed Central
2016
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| Предметы: | |
| Online-ссылка: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4707779/ https://ncbi.nlm.nih.gov/pubmed/26753747 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13059-015-0861-4 |
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