Two novel PRP31 premessenger ribonucleic acid processing factor 31 homolog mutations including a complex insertion-deletion identified in Chinese families with retinitis pigmentosa.

TitleTwo novel PRP31 premessenger ribonucleic acid processing factor 31 homolog mutations including a complex insertion-deletion identified in Chinese families with retinitis pigmentosa.
Publication TypeJournal Article
Year of Publication2013
AuthorsDong B, Chen J, Zhang X, Pan Z, Bai F, Li Y
JournalMolecular vision
Volume19
Pagination2426-35
Date Published2013
Abstract

To identify the causative mutations in two Chinese families with retinitis pigmentosa (RP), and to describe the associated phenotype.

DOI10.1155/2013/865181
Alternate JournalMol. Vis.