Title : Ocular findings associated with rhodopsin gene codon 267 and codon 190 mutations in dominant retinitis pigmentosa.

Pub. Date : 1992 Nov

PMID : 1444916






1 Functional Relationships(s)
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1 Two members of a family with autosomal dominant retinitis pigmentosa were found to have a cytosine-to-thymine mutation in the second nucleotide of codon 267 in the rhodopsin gene that resulted in a proline-to-leucine change. Leucine rhodopsin Homo sapiens