Frequency and origin of the c.2090T>G p.(Leu697Trp) MYO3A variant associated with autosomal dominant hearing loss

European Journal of Human Genetics, Published online: 06 May 2021; doi:10.1038/s41431-021-00891-0Frequency and origin of the c.2090T>G p.(Leu697Trp) MYO3A variant associated with autosomal dominant hearing loss

Source: European Journal of Human Genetics - May 6, 2021 Category: Genetics & Stem Cells Authors: Andr é S. Bueno Kelly Nunes Alex M. M. Dias Leandro U. Alves Beatriz C. A. Mendes Juliana Sampaio-Silva Jeroen Smits Helger G. Yntema Diogo Meyer Karina Lezirovitz Regina C. Mingroni-Netto Source Type: research