Article
1 rhodopsin mutations in congenital night blindness.
Advances in experimental medicine and biology - 1 Jan 2010
McAlear Suzanne D, Kraft Timothy W, Gross Alecia K
Abstract excerpt
While there are over 100 distinct mutations in the rhodopsin gene that are found in patients with the degenerative disease autosomal dominant retinitis pigmentosa (ADRP), there are only four known mutations in the rhodopsin gene found in patients with the dysfunction congenital stationary night blindness (CSNB). CSNB patients have a much less severe phenotype than those with ADRP; the patients only lose rod...
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