Frequency and origin of the c.2090T>G p.(Leu697Trp) MYO3A variant associated with autosomal dominant hearing loss
c.2090T>G p.(Leu697Trp) MYO3A 变异与常染色体显性遗传性听力损失相关,其频率和起源
期刊:European Journal of Human Genetics
影响因子:4.6
doi:10.1038/s41431-021-00891-0
Bueno, André S; Nunes, Kelly; Dias, Alex M M; Alves, Leandro U; Mendes, Beatriz C A; Sampaio-Silva, Juliana; Smits, Jeroen; Yntema, Helger G; Meyer, Diogo; Lezirovitz, Karina; Mingroni-Netto, Regina C