Background
Retinitis pigmentosa (RP) is an inheritable disease characterized by progressive retinal degeneration and loss of rod photoreceptor cells, leading to total blindness. Recently three genes responsible for autosomal dominant RP (HPRP3, PRPF31, and PRPC8) ha
Synonyms
PRPF3; PRP3 pre-mRNA processing factor 3 homolog (S. cerevisiae); PRP3 pre mRNA processing factor 3 homolog (yeast) , retinitis pigmentosa 18 (autosomal dominant) , RP18; U4/U6 small nuclear ribonucleoprotein Prp3; HPRP3; Prp3; U4/U6 snRNP 90 kDa protein; pre-mRNA-splicing factor 3; U4/U6-associated RNA splicing factor; RP18; Prp3p; HPRP3P; HPRP3, HPRP3P, PRP3, Prp3p, RP18, PRPF3; pre-mRNA processing factor 3; PRP3 pre-mRNA processing factor 3 homolog; PRP3 pre-mRNA processing factor 3 homolog (yeast); wu:fa11f05