Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Farnoush ALIAZAMI"'
Autor:
Farnoush ALIAZAMI, Dariush D. FARHUD, Marjan ZARIF-YEGANEH, Siamak SALEHI, Azam HOSSEINIPOUR, Roxana SASANFAR, Maryam Eslami
Publikováno v:
Iranian Journal of Public Health, Vol 49, Iss 11, Pp 2128-2135 (2020)
Background: Hearing loss (HL) is one of the most common heterogeneous congenital disabilities worldwide. Gap junction protein β-3 (GJB3) gene encodes Connexin31 protein (Cx31). The hereditary type of hearing impairment in this gene are known to caus
Externí odkaz:
https://doaj.org/article/cef6a33e24324cc1a0c3b88e77a90d5b
Autor:
Farnoush Aliazami, Sapideh Gilani, Dariush Farhud, Mohsen Naraghi, Mahdi Afshari, Maryam Eslami
Publikováno v:
International Journal of Pediatric Otorhinolaryngology. 168:111512
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c708efc259043c5a3062d374a47dd974
https://doi.org/10.1016/j.ijporl.2023.111512
https://doi.org/10.1016/j.ijporl.2023.111512
Autor:
Maryam Eslami, Marjan Zarif-Yeganeh, Azam Hosseinipour, Farnoush Aliazami, Roxana Sasanfar, Siamak Salehi, Dariush D. Farhud
Publikováno v:
Iranian Journal of Public Health
Iranian Journal of Public Health, Vol 49, Iss 11, Pp 2128-2135 (2020)
Iranian Journal of Public Health, Vol 49, Iss 11, Pp 2128-2135 (2020)
Background: Hearing loss (HL) is one of the most common heterogeneous congenital disabilities worldwide. Gap junction protein β-3 (GJB3) gene encodes Connexin31 protein (Cx31). The hereditary type of hearing impairment in this gene are known to caus
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c314376d34e1e4de255ddcc7fcacf480
http://europepmc.org/articles/PMC7917519
http://europepmc.org/articles/PMC7917519