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A substitution mutation in cardiac ubiquitin ligase, FBXO32, is associated with an autosomal recessive form of dilated cardiomyopathy
Journal article   Open access  Peer reviewed

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

Zuhair N. Al-Hassnan, Zarghuna MA Shinwari, Salma M. Wakil, Sahar Tulbah, Shamayel Mohammed, Zuhair Rahbeeni, Mohammed Alghamdi, Monther Rababh, Dilek Colak, Namik Kaya, …
BMC medical genetics, Vol.17(1), pp.3-3
14/01/2016
DOI: https://doi.org/10.1186/s12881-016-0267-5
PMCID: PMC4714499
PMID: 26768247

Abstract

Cardiomyopathy FBXO32 Ubiquitin proteasome system
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https://doi.org/10.1186/s12881-016-0267-5View
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