Associated Papers
Mutation spectrum of PRPF31, genotype-phenotype correlation in retinitis pigmentosa, and opportunities for therapy.
Wheway G et al.
Experimental Eye Research, 2020
Clinical and genetic identification of a large chinese family with autosomal dominant retinitis pigmentosa.
Yang Y et al.
Ophthalmic Genetics, 2015
A novel PRPF31 mutation in a large Chinese family with autosomal dominant retinitis pigmentosa and macular degeneration.
Lu F et al.
Plos One, 2013
[Novel splice-site mutation in the pre-mRNA splicing gene PRPF31 in a Chinese family with autosomal dominant retinitis pigmentosa].
Lu SS et al.
[zhonghua Yan Ke Za Zhi] Chinese Journal of Ophthalmology, 2005
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