NCOA3 identified as a new candidate to explain autosomal dominant progressive hearing loss

Bibliographic Details
Author: Mingroni Netto, Regina Celia
Format: Article
Status:Published version
Publication date:2020
Country:Brasil
Institution:USP
Repository:Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Language:English
OAI Identifier:003048194
Online Access:https://doi.org/10.1093/hmg/ddaa240
Access Level:Open access
Keyword:MUTAÇÃO GENÉTICA
Description
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