PRPF4 Mutations Cause Autosomal Dominant Retinitis Pigmentosa
Page 1 of 1
PRPF4 Mutations Cause Autosomal Dominant Retinitis Pigmentosa
Jon Moulton Wed Jan 15, 2014 12:00 pm
Chen X, Liu Y, Sheng X, Tam PO, Zhao K, Chen X, Rong W, Liu Y, Liu X, Pan X, Chen LJ, Zhao Q, Vollrath D, Pang CP, Zhao C. PRPF4 Mutations Cause Autosomal Dominant Retinitis Pigmentosa. Hum Mol Genet. 2014 Jan 12. [Epub ahead of print]
Jon Moulton- Posts : 5721
Join date : 2010-03-12
Age : 62
Location : Philomath, Oregon, USA -
Similar topics» Identification of a PRPF4 Loss-of-Function Variant That Abrogates U4/U6.U5 Tri-snRNP Integration and Is Associated with Retinitis Pigmentosa
» SLC7A14 linked to autosomal recessive retinitis pigmentosa
» A mutation in ADIPOR1 causes nonsyndromic autosomal dominant retinitis pigmentosa
» Whole-exome sequencing reveals POC5 as a novel gene associated with autosomal recessive retinitis pigmentosa
» Mutation in the intracellular chloride channel CLCC1 associated with autosomal recessive retinitis pigmentosa
» SLC7A14 linked to autosomal recessive retinitis pigmentosa
» A mutation in ADIPOR1 causes nonsyndromic autosomal dominant retinitis pigmentosa
» Whole-exome sequencing reveals POC5 as a novel gene associated with autosomal recessive retinitis pigmentosa
» Mutation in the intracellular chloride channel CLCC1 associated with autosomal recessive retinitis pigmentosa
Page 1 of 1
Permissions in this forum:
You cannot reply to topics in this forum