X-Linked Cone Dystrophy Caused by Mutation of the Red and Green Cone Opsins-Reference-Cited by-同舟云学术

X-Linked Cone Dystrophy Caused by Mutation of the Red and Green Cone Opsins

Published:2010-07 Issue:1 Volume:87 Page:26-39
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Gardner Jessica C.,Webb Tom R.,Kanuga Naheed,Robson Anthony G.,Holder Graham E.,Stockman Andrew,Ripamonti Caterina,Ebenezer Neil D.,Ogun Olufunmilola,Devery Sophie,Wright Genevieve A.,Maher Eamonn R.,Cheetham Michael E.,Moore Anthony T.,Michaelides Michel,Hardcastle Alison J.

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference69 articles.

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2. X-linked cone-rod dystrophy (locus COD1): identification of mutations in RPGR exon ORF15;Demirci;Am. J. Hum. Genet.,2002

3. Mutations in the RPGR gene cause X-linked cone dystrophy;Yang;Hum. Mol. Genet.,2002

4. Identification of novel RPGR ORF15 mutations in X-linked progressive cone-rod dystrophy (XLCORD) families;Ebenezer;Invest. Ophthalmol. Vis. Sci.,2005

5. RPGR ORF15 genotype and clinical variability of retinal degeneration in an Australian population;Ruddle;Br. J. Ophthalmol.,2009

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