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Keyword [PRPF31]
Result: 1 - 6 | Page: 1 of 1
1.
Gene Mapping And Analysis Of Candidate Genes In Two Chinese Families With Retinitis Pigmentosa
2.
RP33, A Novel Locus Of Autosomal Dominant Retinitis Pigmentosa; And A Complete Mutation Screening Of PRPF31 Gene In RP11 Linked Family
3.
Screening And Functional Identification Of PRPF31 Gene Mutation In Non-syndromic Retinitis Pigmentosa Families
4.
Whole Exome Sequencing Identifiy Novel PRPF31 Mutations In RP And Function Study Of EMC9 Of RP Causitive Gene
5.
The Mechanism Underlying Prpf31 Deficiency-induced Retinal Development Defect And Retinitis Pigmentosa
6.
AAV-mediated PRPF31 Gene Augmentation Prevents Retinal Degeneration In A Mouse Model Of Retinitis Pigmentosa
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