← Evidence map

ArticleAmerican journal of human genetics2009

Recessive mutations of the gene TRPM1 abrogate ON bipolar cell function and cause complete congenital stationary night blindness in humans.

Zheng Li et al.PubMed ↗Full text ↗Publisher ↗

No numbers read from the abstract.

114 papers cite itlatest 60 shown

2009
…
2016
2017
2018
2019
2020
2021
2022
2023
2024
2025
2026
this paperpooled itcites it
Full record →Abstract, authors, funding and every citing paper · PMID 19878917