Aberrant regulation of epigenetic modifiers contributes to the pathogenesis in patients with selenoprotein N-related myopathies
表观遗传修饰因子的异常调控是硒蛋白N相关肌病患者发病机制的促成因素。
期刊:Human Mutation
影响因子:3.7
doi:10.1002/humu.23745
Bachmann, Christoph; Noreen, Faiza; Voermans, Nicol C; Schär, Primo L; Vissing, John; Fock, Johanna M; Bulk, Saskia; Kusters, Benno; Moore, Steven A; Beggs, Alan H; Mathews, Katherine D; Meyer, Megan; Genetti, Casie A; Meola, Giovanni; Cardani, Rosanna; Mathews, Emma; Jungbluth, Heinz; Muntoni, Francesco; Zorzato, Francesco; Treves, Susan
