Rare coding variants involving MYO7A and other genes encoding stereocilia link proteins in familial meniere disease
FI: 3,208
Type: Article
Artículo original
Year: 2021
Writers
Roman-Naranjo, P; Moleon, MDC; Aran, I; Escalera-Balsera, A; Soto-Varela, A; Bachinger, D; Gomez-Finana, M; Eckhard, AH; Lopez-Escamez, J.A.
Magazine
Title: HEARING RESEARCH
Quartile
- D1