OTOF mutations revealed by genetic analysis of hearing loss families including a potential temperature sensitive auditory neuropathy allele

Autor: Varga, R, Avenarius, MR, Kelley, PM, Keats, BJ, Berlin, CI, Hood, LJ, Morlet, TG, Brashears, SM, Starr, A, Cohn, ES, Smith, RJH, Kimberling, WJ

Publikováno v: Varga, R; Avenarius, MR; Kelley, PM; Keats, BJ; Berlin, CI; Hood, LJ; et al.(2006). OTOF mutations revealed by genetic analysis of hearing loss families including a potential temperature sensitive auditory neuropathy allele. Journal of Medical Genetics, 43(7), 576-581. doi: 10.1136/jmg.2005.038612. UC Irvine: Retrieved from: http://www.escholarship.org/uc/item/4m09d687

Introduction: The majority of hearing loss in children can be accounted for by genetic causes. Non-syndromic hearing loss accounts for 80% of genetic hearing loss in children, with mutations in DFNB1/GJB2 being by far the most common cause. Among the

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od_______325::6087e5bee4224547e358f32758219e73
http://www.escholarship.org/uc/item/4m09d687

OTOF mutations revealed by genetic analysis of hearing loss families including a potential temperature sensitive auditory neuropathy allele.

Autor: Varga R; Center for Hereditary Communication Disorders, Boys Town National Research Hospital (BTNRH), Omaha, NE, USA., Avenarius MR, Kelley PM, Keats BJ, Berlin CI, Hood LJ, Morlet TG, Brashears SM, Starr A, Cohn ES, Smith RJ, Kimberling WJ

Publikováno v: Journal of medical genetics [J Med Genet] 2006 Jul; Vol. 43 (7), pp. 576-81. Date of Electronic Publication: 2005 Dec 21.