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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Bibliografski detalji
Izdano u:Genome Biol
Glavni autori: Al-Yacoub, Nadya, Shaheen, Ranad, Awad, Salma Mahmoud, Kunhi, Muhammad, Dzimiri, Nduna, Nguyen, Henry C., Xiong, Yong, Al-Buraiki, Jehad, Al-Habeeb, Waleed, Alkuraya, Fowzan S., Poizat, Coralie
Format: Artigo
Jezik:Inglês
Izdano: BioMed Central 2016
Teme:
Research
Online pristup: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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