A substitution mutation in cardiac ubiquitin ligase, FBXO32, is associated with an autosomal recessive form of dilated cardiomyopathy
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,Volume:
17
Language:
english
Journal:
BMC Medical Genetics
DOI:
10.1186/s12881-016-0267-5
Date:
December, 2016
File:
PDF, 2.63 MB
english, 2016