← Evidence map

ArticleJournal of human genetics2017

Exome sequencing identifies POU4F3 as the causative gene for a large Chinese family with non-syndromic hearing loss.

Xin Zhang Cai et al.PubMed ↗Publisher ↗

No numbers read from the abstract.

21 papers cite it

2016
2017
2018
2019
2020
2021
2022
2023
this papercites it
Full record →Abstract, authors, funding and every citing paper · PMID 27535032