A substitution mutation in cardiac ubiquitin ligase, FBXO32, is associated with an autosomal recessive form of dilated cardiomyopathy
心脏泛素连接酶FBXO32的替换突变与常染色体隐性遗传的扩张型心肌病相关。
期刊:BMC Medical Genetics
影响因子:
doi:10.1186/s12881-016-0267-5
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