A six-generation Chinese family in haplogroup B4C1C exhibits high penetrance of 1555A > G-induced hearing Loss

• Prif Awduron: Bai Yan (Awdur), Wang Zhengmin (Awdur), Dai Wenjia (Awdur), Li Qingzhong (Awdur), Chen Guoling (Awdur), Cong Ning (Awdur), Guan Minxin (Awdur), Li Huawei (Awdur)
• Fformat: Llyfr
• Cyhoeddwyd: BMC, 2010-09-01T00:00:00Z.
• Pynciau: article
• Mynediad Ar-lein: Connect to this object online.

<p>Abstract</p> <p>Background</p> <p>The 1555A > G mutation is the most common cause of aminoglycoside-induced and non-syndromic deafness. However, the variable clinical phenotype and incomplete penetrance of A1555G-induced hearing loss complicate our understanding o...