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pro vyhledávání: '"Bang-Qing Huang"'
Autor:
Yu Su, Xue Gao, Sha-Sha Huang, Jing-Ning Mao, Bang-Qing Huang, Jian-Dong Zhao, Dong-Yang Kang, Xin Zhang, Pu Dai
Publikováno v:
BMC Medical Genetics, Vol 19, Iss 1, Pp 1-10 (2018)
Abstract Background Many X-linked non-syndromic hearing loss (HL) cases are caused by various mutations in the POU domain class 3 transcription factor 4 (POU3F4) gene. This study aimed to identify allelic variants of this gene in two Chinese families
Externí odkaz:
https://doaj.org/article/604998c83ad14c2fb6a45300b70057d4
Publikováno v:
Journal of otology. 10(2)
Based on the clinical manifestations of a hearing loss patient, theA comprehensive physical examination was performed on the proband to exclude abnormalities of other organs, and detailed audiological testing and temporal bone CT scan were also perfo