Retinal and renal complications in patients with a mutation of mitochondrial DNA at position 3,243 (maternally inherited diabetes and deafness). A case

Retinal and renal complications in patients with a mutation of mitochondrial DNA at position 3,243 (maternally inherited diabetes and deafness). A case–control study

Published:2008-06-26 Issue:9 Volume:51 Page:1664-1670
ISSN:0012-186X
Container-title:Diabetologia
language:en
Short-container-title:Diabetologia

Author:

Massin P.,Dubois-Laforgue D.,Meas T.,Laloi-Michelin M.,Gin H.,Bauduceau B.,Bellanné-Chantelot C.,Bertin E.,Blickle J.-F.,Bouhanick B.,Cahen-Varsaux J.,Casanova S.,Charpentier G.,Chedin P.,Dupuy O.,Grimaldi A.,Guerci B.,Kaloustian E.,Lecleire-Collet A.,Lorenzini F.,Murat A.,Narbonne H.,Olivier F.,Paquis-Flucklinger V.,Virally M.,Vincenot M.,Vialettes B.,Timsit J.,Guillausseau P. J.,

Publisher

Springer Science and Business Media LLC

Subject

Endocrinology, Diabetes and Metabolism,Internal Medicine

Link

http://link.springer.com/content/pdf/10.1007/s00125-008-1073-1.pdf

Reference39 articles.

1. Van den Ouweland JMW, Lemkes HHPJ, Ruittenbeek W et al (1992) Mutation in mitochondrial tRNALeu(UUR) gene in a large pedigree with maternally transmitted type II diabetes mellitus and deafness. Nat Genet 1:368–371

2. Reardon W, Ross RJM, Sweeney MG et al (1992) Diabetes mellitus associated with a pathogenic point mutation in mitochondrial DNA. Lancet 340:1376–1379

3. Guillausseau PJ, Massin P, Dubois-Laforgue D et al (2001) Maternally inherited diabetes and deafness: a multicenter survey. Ann Intern Med 134:721–728

4. Massin P, Guillausseau PJ, Vialettes B et al (1995) Macular pattern dystrophy associated with a mutation of mitochondrial DNA. Am J Ophthalmol 120:247–248

5. Massin P, Virally-Monod M, Vialettes B et al (1999) Prevalence of macular pattern dystrophy in maternally inherited diabetes and deafness. Ophthalmology 106:1821–1827

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