Whole-exome sequencing links a variant in DHDDS to retinitis pigmentosa
Page 1 of 1
Whole-exome sequencing links a variant in DHDDS to retinitis pigmentosa
Jon Moulton Wed Aug 17, 2011 4:33 pm
Züchner S, Dallman J, Wen R, Beecham G, Naj A, Farooq A, Kohli MA, Whitehead PL, Hulme W, Konidari I, Edwards YJ, Cai G, Peter I, Seo D, Buxbaum JD, Haines JL, Blanton S, Young J, Alfonso E, Vance JM, Lam BL, Peričak-Vance MA. Whole-exome sequencing links a variant in DHDDS to retinitis pigmentosa. Am J Hum Genet. 2011 Feb 11;88(2):201-6. Epub 2011 Feb 3.
Jon Moulton- Posts : 5721
Join date : 2010-03-12
Age : 61
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
» Whole-exome sequencing reveals POC5 as a novel gene associated with autosomal recessive retinitis pigmentosa
» Retinitis Pigmentosa Gene, C2ORF71
» SLC7A14 linked to autosomal recessive retinitis pigmentosa
» PRPF4 Mutations Cause Autosomal Dominant Retinitis Pigmentosa
» Whole-exome sequencing reveals POC5 as a novel gene associated with autosomal recessive retinitis pigmentosa
» Retinitis Pigmentosa Gene, C2ORF71
» SLC7A14 linked to autosomal recessive retinitis pigmentosa
» PRPF4 Mutations Cause Autosomal Dominant Retinitis Pigmentosa
Page 1 of 1
Permissions in this forum:
You cannot reply to topics in this forum|
|
|