Variability in clinical phenotypes of PRPF8 -linked autosomal dominant retinitis pigmentosa correlates with differential PRPF8/SNRNP200 interactions
Escher, Pascal, Passarin, Olga, Munier, Francis L., Tran, Viet H., Vaclavik, VeronikaLanguage:
english
Journal:
Ophthalmic Genetics
DOI:
10.1080/13816810.2017.1393825
Date:
October, 2017
File:
PDF, 1.31 MB
english, 2017