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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Dettagli Bibliografici
Pubblicato in:Genome Biol
Autori principali: 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
Natura: Artigo
Lingua:Inglês
Pubblicazione: BioMed Central 2016
Soggetti:
Research
Accesso online: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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