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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Detalles Bibliográficos
Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4707779/
https://www.ncbi.nlm.nih.gov/pubmed/26753747
http://dx.doi.org/10.1186/s13059-015-0861-4

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4707779/
https://www.ncbi.nlm.nih.gov/pubmed/26753747
http://dx.doi.org/10.1186/s13059-015-0861-4

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