Identification of a PRPF4 Loss-of-Function Variant That Abrogates U4/U6.U5 Tri-snRNP Integration and Is Associated with Retinitis Pigmentosa
Page 1 of 1
Identification of a PRPF4 Loss-of-Function Variant That Abrogates U4/U6.U5 Tri-snRNP Integration and Is Associated with Retinitis Pigmentosa
Linder B, Hirmer A, Gal A, Rüther K, Bolz HJ, Winkler C, Laggerbauer B, Fischer U. Identification of a PRPF4 Loss-of-Function Variant That Abrogates U4/U6.U5 Tri-snRNP Integration and Is Associated with Retinitis Pigmentosa. PLoS ONE. 2014;9(11):e111754. doi:10.1371/journal.pone.0111754
Similar topics
» PRPF4 Mutations Cause Autosomal Dominant Retinitis Pigmentosa
» Whole-exome sequencing links a variant in DHDDS to retinitis pigmentosa
» Retinitis Pigmentosa Gene, C2ORF71
» SLC7A14 linked to autosomal recessive retinitis pigmentosa
» The Role of Mislocalized Phototransduction in Photoreceptor Cell Death of Retinitis Pigmentosa
» Whole-exome sequencing links a variant in DHDDS to retinitis pigmentosa
» Retinitis Pigmentosa Gene, C2ORF71
» SLC7A14 linked to autosomal recessive retinitis pigmentosa
» The Role of Mislocalized Phototransduction in Photoreceptor Cell Death of Retinitis Pigmentosa
Page 1 of 1
Permissions in this forum:
You cannot reply to topics in this forum
|
|