Rare coding variants involving MYO7A and other genes encoding stereocilia link proteins in familial meniere disease

  1. Roman-Naranjo, P.
  2. Moleon, M.D.C.
  3. Aran, I.
  4. Escalera-Balsera, A.
  5. Soto-Varela, A.
  6. Bächinger, D.
  7. Gomez-Fiñana, M.
  8. Eckhard, A.H.
  9. Lopez-Escamez, J.A.
Revista:
Hearing Research

ISSN: 1878-5891 0378-5955

Ano de publicación: 2021

Volume: 409

Tipo: Artigo

DOI: 10.1016/J.HEARES.2021.108329 GOOGLE SCHOLAR lock_openAcceso aberto editor