Residual Hearing in DFNB1 Deafness and Its Clinical Implication in a Korean Population

Author:

Kim So Young,Kim Ah Reum,Han Kyu Hee,Kim Min Young,Jeon Eun-Hee,Koo Ja-Won,Oh Seung Ha,Choi Byung Yoon

Publisher

Public Library of Science (PLoS)

Subject

Multidisciplinary

Reference40 articles.

1. Newborn hearing screening—a silent revolution;CC Morton;The New England journal of medicine,2006

2. Epidemiological studies on hearing impairment with reference to genetic factors in Sichuan, China;XZ Liu;The Annals of otology, rhinology, and laryngology,2001

3. Connexin 26 mutations in hereditary non-syndromic sensorineural deafness;DP Kelsell;Nature,1997

4. Estivill X, Gasparini P, The Connexin-deafness homepage, Deafness Research Group (DRG). Available: http://http://davinci.crg.es/deafness/1/27/2015.

5. GJB2 mutations and degree of hearing loss: a multicenter study;RL Snoeckx;American journal of human genetics,2005

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