A substitution mutation in cardiac ubiquitin ligase, FBXO32, is associated with an autosomal recessive form of dilated cardiomyopathy

BACKGROUND: Familial dilated cardiomyopathy (DCM) is genetically heterogeneous. Mutations in more than 40 genes have been identified in familial cases, mostly inherited in an autosomal dominant pattern. DCM due to recessive mutations is rarely observed. In consanguineous families, homozygosity mappi...

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Detalles Bibliográficos
Autores principales: Al-Hassnan, Zuhair N., Shinwari, Zarghuna MA., Wakil, Salma M., Tulbah, Sahar, Mohammed, Shamayel, Rahbeeni, Zuhair, Alghamdi, Mohammed, Rababh, Monther, Colak, Dilek, Kaya, Namik, Al-Fayyadh, Majid, Alburaiki, Jehad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4714499/
https://www.ncbi.nlm.nih.gov/pubmed/26768247
http://dx.doi.org/10.1186/s12881-016-0267-5

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4714499/
https://www.ncbi.nlm.nih.gov/pubmed/26768247
http://dx.doi.org/10.1186/s12881-016-0267-5

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