← Evidence map

ArticleOphthalmology2014

Whole exome sequencing identifies CRB1 defect in an unusual maculopathy phenotype.

Stephen H Tsang et al.PubMed ↗Full text ↗Publisher ↗

No numbers read from the abstract.

40 papers cite it

2014
2015
2016
2017
2018
2019
2020
2021
2022
2023
2024
2025
2026
this papercites it
Full record →Abstract, authors, funding and every citing paper · PMID 24811962