Associated Papers
Unique pore architecture underlies constitutive gating of human retinal TRPM1.
Sharma M et al.
Biorxiv : the Preprint Server for Biology, 2026
Congenital stationary night blindness: an analysis and update of genotype-phenotype correlations and pathogenic mechanisms.
Zeitz C et al.
Progress in Retinal and Eye Research, 2015
Transient receptor potential genes and human inherited disease.
Everett KV
Advances in Experimental Medicine and Biology, 2011
TRPM1 is mutated in patients with autosomal-recessive complete congenital stationary night blindness.
Audo I et al.
American Journal of Human Genetics, 2009
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