作者
Sobha Sivaprasad,Boom Ting Kung,Anthony G. Robson,Graeme Black,Andrew R. Webster,Alan C. Bird,Catherine Egan
摘要
Clinical & Experimental OphthalmologyVolume 36, Issue 1 p. 92-93 A new phenotype of macular dystrophy associated with a mitochondrial A3243G mutation Sobha Sivaprasad FRCS, Sobha Sivaprasad FRCS Moorfields Eye Hospital, London, andSearch for more papers by this authorBoom Ting Kung MBBS, Boom Ting Kung MBBS Moorfields Eye Hospital, London, andSearch for more papers by this authorAnthony G Robson PhD, Anthony G Robson PhD Moorfields Eye Hospital, London, andSearch for more papers by this authorGraeme Black FRCOphth, Graeme Black FRCOphth Department of Clinical Genetics, St Mary's Hospital, Manchester, UKSearch for more papers by this authorAndrew R Webster FRCOphth, Andrew R Webster FRCOphth Moorfields Eye Hospital, London, andSearch for more papers by this authorAlan Bird FRCOphth, Alan Bird FRCOphth Moorfields Eye Hospital, London, andSearch for more papers by this authorCatherine Egan FRANZCO, Catherine Egan FRANZCO Moorfields Eye Hospital, London, andSearch for more papers by this author Sobha Sivaprasad FRCS, Sobha Sivaprasad FRCS Moorfields Eye Hospital, London, andSearch for more papers by this authorBoom Ting Kung MBBS, Boom Ting Kung MBBS Moorfields Eye Hospital, London, andSearch for more papers by this authorAnthony G Robson PhD, Anthony G Robson PhD Moorfields Eye Hospital, London, andSearch for more papers by this authorGraeme Black FRCOphth, Graeme Black FRCOphth Department of Clinical Genetics, St Mary's Hospital, Manchester, UKSearch for more papers by this authorAndrew R Webster FRCOphth, Andrew R Webster FRCOphth Moorfields Eye Hospital, London, andSearch for more papers by this authorAlan Bird FRCOphth, Alan Bird FRCOphth Moorfields Eye Hospital, London, andSearch for more papers by this authorCatherine Egan FRANZCO, Catherine Egan FRANZCO Moorfields Eye Hospital, London, andSearch for more papers by this author First published: 17 February 2008 https://doi.org/10.1111/j.1442-9071.2007.01656.xCitations: 1Read the full textAboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Share a linkShare onEmailFacebookTwitterLinkedInRedditWechat References 1 Bellmann C, Neveu MM, Scholl HP et al. Localized retinal electrophysiological and fundus autofluorescence imaging abnormalities in maternal inherited diabetes and deafness invest. Ophthalmol Vis Sci 2004; 45: 2355–60. 2 Massin P, Virally-Monod M, Vialettes B et al. Prevalence of macular pattern dystrophy in maternally inherited diabetes and deafness. GEDIAM Group. Ophthalmology 1999; 106: 1821–7. 3 Guillausseau PJ, Massin P, Dubois-LaForgue D et al. Maternally inherited diabetes and deafness: a multicenter study. Ann Intern Med 2001 May 1; 134 (9 Pt 1): 721–8. 4 Harrison TJ, Boles RG, Johnson DR, LeBlond C, Wong LJ. Macular pattern retinal dystrophy, adult-onset diabetes, and deafness: a family study of A3243G mitochondrial heteroplasmy. Am J Ophthalmol 1997; 124: 217–21. Citing Literature Volume36, Issue1January/February 2008Pages 92-93 ReferencesRelatedInformation