Tel: 1-631-626-9181 (USA)   44-208-144-6005 (Europe)


Official Full Name
pre-mRNA processing factor 3
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
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

Interested in learning more?

Contact us today for a free consultation with the scientific team and discover how Creative Biogene can be a valuable resource and partner for your organization.

Request a quote today!