https://disorders.eyes.arizona.edu/references/mutations-trpm1-are-common-cause-complete-congenital-stationary-night-blindness
Mutations in TRPM1 are a common cause of complete congenital stationary night blindness |...
https://pubchem.ncbi.nlm.nih.gov/gene/TRPM1
TRPM1 | Gene Target - PubChem
Gene target information for TRPM1. Find diseases associated with this biological target and compounds tested against it in bioassay experiments.
genetargetpubchem
https://pubmed.ncbi.nlm.nih.gov/22896717/
Depolarizing bipolar cell dysfunction due to a Trpm1 point mutation
Mutations in TRPM1 are found in humans with an autosomal recessive form of complete congenital stationary night blindness (cCSNB). The Trpm1(-/-) mouse has...
due tobipolarcelldysfunctionpoint
https://channelpedia.epfl.ch/wikipages/165
Channelpedia - TRPM1