Xcode Life

Condition: Retinitis Pigmentosa 13

rs1555550617 in PRPF8 gene and Retinitis Pigmentosa 13

PMID 24938718 2014 Mutations of 60 known causative genes in 157 families with retinitis pigmentosa based on exome sequencing.

rs121434240 in PRPF8;RILP gene and Retinitis Pigmentosa 13

PMID 17317632 2007 Structure of a multipartite protein-protein interaction domain in splicing factor prp8 and its link to retinitis pigmentosa.

PMID 12714658 2003 Mutations in the pre-mRNA splicing-factor genes PRPF3, PRPF8, and PRPF31 in Spanish families with autosomal dominant retinitis pigmentosa.

PMID 11468273 2001 Mutations in the pre-mRNA splicing factor gene PRPC8 in autosomal dominant retinitis pigmentosa (RP13).

PMID 11910553 2002 Clinical characterization, linkage analysis, and PRPC8 mutation analysis of a family with autosomal dominant retinitis pigmentosa type 13 (RP13).

rs121434236 in RILP;PRPF8 gene and Retinitis Pigmentosa 13

PMID 17317632 2007 Structure of a multipartite protein-protein interaction domain in splicing factor prp8 and its link to retinitis pigmentosa.

PMID 11468273 2001 Mutations in the pre-mRNA splicing factor gene PRPC8 in autosomal dominant retinitis pigmentosa (RP13).

PMID 12714658 2003 Mutations in the pre-mRNA splicing-factor genes PRPF3, PRPF8, and PRPF31 in Spanish families with autosomal dominant retinitis pigmentosa.

PMID 11910553 2002 Clinical characterization, linkage analysis, and PRPC8 mutation analysis of a family with autosomal dominant retinitis pigmentosa type 13 (RP13).