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Article

A novel de novo mutation of ACTG1 in two sporadic non-syndromic hearing loss cases.

Science China. Life sciences - 1 Jun 2018

Wang Hongyang, Guan Jing, Lan Lan, Yu Lan, Xie Linyi, Liu Xu, Yang Ju, Zhao Cui, Wang Dayong, Wang Qiuju

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Source

Identifiers

PMID: 29357087
DOI: 10.1007/s11427-017-9165-2

Genes

ACTG1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

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