A novel POU domain class 3 transcription factor 4 mutation causes X-linked non-syndromic hearing loss in a Chinese family

Chin Med J (Engl). 2019 Sep 20;132(18):2251-2253. doi: 10.1097/CM9.0000000000000425.

Authors

Hong-Min Wu¹, Hui-Qun Jie¹, Hui Wang¹, Ya-Qin Wu¹, Zheng-Nong Chen¹, Ya-Zhi Xing¹, Ji-Ping Wang¹, Hai-Bo Shi^{1

2}, Shan-Kai Yin^{1

2}

Affiliations

¹ Department of Otolaryngology, Sixth People's Hospital, Shanghai Jiao Tong University, Otolaryngology Institute of Shanghai Jiao Tong University, Shanghai 200233, China.
² Shanghai Key Laboratory of Sleep Disordered Breathing, Shanghai 200233, China.

No abstract available

MeSH terms

Adult
Apoptosis Inducing Factor / genetics
Asian People / genetics
Collagen Type IV / genetics
Hearing Loss, Sensorineural / genetics*
Humans
Male
Mutation / genetics
POU Domain Factors / genetics
Ribose-Phosphate Pyrophosphokinase / genetics
Transcription Factor 4 / genetics*
Young Adult

Substances

AIFM1 protein, human
Apoptosis Inducing Factor
COL4A6 protein, human
Collagen Type IV
POU Domain Factors
POU3F4 protein, human
TCF4 protein, human
Transcription Factor 4
PRPS1 protein, human
Ribose-Phosphate Pyrophosphokinase