Characterization of a novel MYO3A missense mutation associated with a dominant form of late onset hearing loss
对一种与显性遗传性迟发性听力损失相关的新型MYO3A错义突变进行表征
期刊:Scientific Reports
影响因子:3.9
doi:10.1038/s41598-018-26818-2
Dantas, Vitor G L; Raval, Manmeet H; Ballesteros, Angela; Cui, Runjia; Gunther, Laura K; Yamamoto, Guilherme L; Alves, Leandro Ucela; Bueno, André Silva; Lezirovitz, Karina; Pirana, Sulene; Mendes, Beatriz C A; Yengo, Christopher M; Kachar, Bechara; Mingroni-Netto, Regina C