Thyroid stimulating hormone receptor novel mutation results in familial hereditary hearing loss

J Biol Regul Homeost Agents. 2020 Jan-Feb;34(1):181-185. doi: 10.23812/19-346-L.

Authors

H Wang¹, L Sun², S Zhou¹

Affiliations

¹ Henan Research Institute of Population and Family Planning, National Health Commission Key Laboratory of Birth Defect Prevention, Jinshui, Zhengzhou, China.
² Translational Medical Center, Zhengzhou Central Hospital, Zhengzhou, Henan Province, P. R. China.

PMID: 32174093
DOI: 10.23812/19-346-L

No abstract available

Keywords: familial hereditary hearing loss; novel mutation; whole exome sequencing.

MeSH terms

Hearing Loss, Sensorineural / genetics*
Humans
Mutation
Receptors, Thyrotropin / genetics*

Substances

Receptors, Thyrotropin