retinitis pigmentosa 9 (autosomal dominant), isoform CRA_c [Homo sapie - Protein

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Mutations in a protein target of the Pim-1 kinase associated with the RP9 form of autosomal dominant retinitis pigmentosa. [Eur J Hum Genet. 2002]
Mutations in a protein target of the Pim-1 kinase associated with the RP9 form of autosomal dominant retinitis pigmentosa.
Keen TJ, Hims MM, McKie AB, Moore AT, Doran RM, Mackey DA, Mansfield DC, Mueller RF, Bhattacharya SS, Bird AC, et al. Eur J Hum Genet. 2002 Apr; 10(4):245-9.
Exclusion of CAG repeat expansion as the cause of disease in autosomal dominant retinitis pigmentosa families. [J Med Genet. 1997]
Exclusion of CAG repeat expansion as the cause of disease in autosomal dominant retinitis pigmentosa families.
Keen TJ, Morris AG, Inglehearn CF. J Med Genet. 1997 Feb; 34(2):130-2.
A YAC contig spanning the dominant retinitis pigmentosa locus (RP9) on chromosome 7p. [Genomics. 1995]
A YAC contig spanning the dominant retinitis pigmentosa locus (RP9) on chromosome 7p.
Keen TJ, Inglehearn CF, Green ED, Cunningham AF, Patel RJ, Peacock RE, Gerken S, White R, Weissenbach J, Bhattacharya SS. Genomics. 1995 Aug 10; 28(3):383-8.

RefSeq genomic sequence
See the genomic reference sequence for the RP9 gene (NG_012968.1).
RefSeq protein isoforms
See 3 reference sequence protein isoforms for the RP9 gene.

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Protein