← Evidence map

ArticleBMC medical genetics2020

Whole exome sequencing identified mutations causing hearing loss in five consanguineous Pakistani families.

Yingjie Zhou et al.PubMed ↗Full text ↗Publisher ↗

No numbers read from the abstract.

11 papers cite it

2020
2021
2022
2023
2024
2025
2026
this papercites it
Full record →Abstract, authors, funding and every citing paper · PMID 32682410