TY  - JOUR
AU  - Roman-Naranjo, P
AU  - Moleon, M D C
AU  - Aran, I
AU  - Escalera-Balsera, A
AU  - Soto-Varela, A
AU  - Bächinger, D
AU  - Gomez-Fiñana, M
AU  - Eckhard, A H
AU  - Lopez-Escamez, J A
PY  - 2021
DO  - 10.1016/j.heares.2021.108329
UR  - http://hdl.handle.net/10668/18378
T2  - Hearing research
AB  - The MYO7A gene encodes a motor protein with a key role in the organization of stereocilia in auditory and vestibular hair cells. Rare variants in the MYO7A (myosin VIIA) gene may cause autosomal dominant (AD) or autosomal recessive (AR) sensorineural...
LA  - en
PB  - Elsevier BV
KW  - Genomics
KW  - Hearing loss
KW  - Inner ear
KW  - Meniere's disease
KW  - Vestibular disorders
KW  - Hair Cells, Vestibular
KW  - Heterozygote
KW  - Humans
KW  - Meniere Disease
KW  - Mutation
KW  - Myosin VIIa
KW  - Pedigree
KW  - Stereocilia
KW  - Usher Syndromes
TI  - Rare coding variants involving MYO7A and other genes encoding stereocilia link proteins in familial meniere disease.
TY  - research article
VL  - 409
ER  -