A biallelic loss-of-function variant in MYZAP is associated with a recessive form of severe dilated cardiomyopathy
MYZAP 中的双等位基因功能丧失变异与严重扩张型心肌病的隐性形式相关
期刊:Cold Spring Harbor Molecular Case Studies
影响因子:1.8
doi:10.1101/mcs.a006221
Ales Maver, Tamara Zigman, Ashraf Yusuf Rangrez, Marijana Coric, Jan Homolak, Dalibor Saric, Iva Skific, Mario Udovicic, Marija Zekusic, Umber Saleem, Sandra D Laufer, Arne Hansen, Norbert Frey, Ivo Baric, Borut Peterlin1