位置：成果数据库 > 期刊 > 期刊详情页
Mutation Spectrum of CommonDeafness-Causing Genes in Patients with Non-Syndromic Deafness in the Xia
  • 期刊名称：PLoS One
  • 时间：2015.8.12
  • 页码：1-12
  • 相关项目：线粒体DNA A1555G遗传学及起源性分析
作者： Xu X|Li R|Han D|Dai P|
同期刊论文项目
线粒体DNA A1555G遗传学及起源性分析
期刊论文 19
同项目期刊论文
The Relationship between the p.V37I Mutation in GJB2 and Hearing Phenotypes in Chinese Individuals.
Rapid identification of aminoglycoside-induced deafness gene mutationsusing multiplex real-time poly
Targeted gene capture and massively parallel sequencing identify TMC1 asthe causative gene in a six-
KCNJ10 may not be a Contributor to Nonsyndromic Enlargement of Vestibular Aqueduct (NSEVA) in Chines
GJB2显性突变在中国耳聋人群中的分布及表型分析
GJB2结构功能及致病机制研究
携带GJB2单杂合突变非综合征型耳聋患者GJA1突变分析
遗传性耳聋家庭康复与预防模式的探讨
单侧大前庭水管综合征SLC26A4基因的突变分析
Impact of next-generation sequencing on molecular diagnosis of inherited non-syndromic hearing loss
双基因突变致聋病例分析