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Paper Details

A monogenic dominant mutation in Rom1 generated by N-ethyl-N-nitrosourea mutagenesis causes retinal degeneration in mice.
Mol Vis
17
2010
(Rho) mRNA, /, Arg, M-1156, M-1156 mutant, M96760, N-ethyl-N-nitrosourea, Prph2, Rgsc1156, Rho protein, Rom1, Rom1(Rgsc1156) mutants, T-->C substitution at position 1, Trp, Trp to Arg substitution at position 182, Trp182Arg, Trp182Arg mutant Rom1, chromosome, mice, mouse, mutant allele, mutant gene, narrowed arteries, peripherin, peripherin/rds (Prph2) mRNA, photoreceptor, photoreceptor degeneration, photoreceptors, position 1,195, rds, retinal degeneration, rhodopsin, rod outer segment membrane protein 1, translated protein, wild-type Prph2

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Release 1.2