trié(s) par (Pertinence décroissant(e), Titre croissant(e)) 

Article

GJB2 p.V37I Mutation Associated With Moderate Nonsyndromic Hearing Loss in an Adult Taiwanese Population

Ting-Ting Yen ; I-Chieh Chen ; Sudi Cho ; Ting-Gang Chang ; Kai-Hsiang Shih ; Men-Wei Hua ; Jui-Lin Li ; Chiann-Yi Hsu ; Tzu-Hung Hsiao ; Yi-Ming Chen |

Dans Ear and hearing (Vol. 44, n°6, November December 2023)

Background: Gap junction protein beta 2 (GJB2) p.V37I mutations are the most important hereditary cause of sensorineural hearing loss (SNHL) in Taiwan. Hearing outcomes are associated with hearing levels at baseline and the duration of follow-up[...]

Plus d'information... En ligne