Clinical, histological and genetic characterization of reducing body myopathy caused by mutations in FHL1.
FHL1基因突变引起的还原体肌病的临床、组织学和遗传学特征
期刊:Brain
影响因子:11.7
doi:10.1093/brain/awn325
Schessl Joachim, Taratuto Ana L, Sewry Caroline, Battini Roberta, Chin Steven S, Maiti Baijayanta, Dubrovsky Alberto L, Erro Marcela G, Espada Graciela, Robertella Monica, Saccoliti Maria, Olmos Patricia, Bridges Leslie R, Standring Peter, Hu Ying, Zou Yaqun, Swoboda Kathryn J, Scavina Mena, Goebel Hans-Hilmar, Mitchell Christina A, Flanigan Kevin M, Muntoni Francesco, Bönnemann Carsten G
