← Evidence map

ArticleBMC ophthalmology2020

Mutation screening of the USH2A gene reveals two novel pathogenic variants in Chinese patients causing simplex usher syndrome 2.

Chenhao He et al.PubMed ↗Full text ↗Publisher ↗

No numbers read from the abstract.

3 papers cite it

2020
2021
this papercites it
Full record →Abstract, authors, funding and every citing paper · PMID 32093671