Characterization of a novel MYO3A missense mutation associated with a dominant form of late onset hearing loss.
Dantas VGL, Raval MH, Ballesteros A, Cui R, Gunther LK, Yamamoto GL, Alves LU, Bueno AS, Lezirovitz K, Pirana S, Mendes BCA, Yengo CM, Kachar B, Mingroni-Netto RC.
Dantas VGL, et al. Among authors: gunther lk.
Sci Rep. 2018 Jun 7;8(1):8706. doi: 10.1038/s41598-018-26818-2.
Sci Rep. 2018.
PMID: 29880844
Free PMC article.
Clinical Trial.