Heterogeneity of diabetes phenotype in patients with 3243 bp mutation of mitochondrial DNA (Maternally Inherited Diabetes and Deafness or MIDD)-Reference-Cited by-同舟云学术

Heterogeneity of diabetes phenotype in patients with 3243 bp mutation of mitochondrial DNA (Maternally Inherited Diabetes and Deafness or MIDD)

Published:2004-04 Issue:2 Volume:30 Page:181-186
ISSN:1262-3636
Container-title:Diabetes & Metabolism
language:en
Short-container-title:Diabetes & Metabolism

Author:

Guillausseau PJ,Dubois-Laforgue D,Massin P,Laloi-Michelin M,Bellanné-Chantelot C,Gin H,Bertin E,Blickle JF,Bauduceau B,Bouhanick B,Cahen-Varsaux J,Casanova S,Charpentier G,Chedin P,Derrien C,Grimaldi A,Guerci B,Kaloustian E,Lorenzini F,Murat A,Olivier F,Paques M,Paquis-Flucklinger V,Tielmans A,Vincenot M,Vialettes B,Timsit J

Publisher

Elsevier BV

Subject

Endocrinology,General Medicine,Endocrinology, Diabetes and Metabolism,Internal Medicine

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3. Mutation in mitochondrial tRNALeu (UUR) gene in a large pedigree with maternally transmitted type II diabetes mellitus and deafness;Van den Ouweland;Nat Genet,1992

4. Diabetes mellitus associated with a pathogenic point mutation in mitochondrial DNA;Reardon;Lancet,1992

5. Maternally inherited diabetes and deafness: a multicenter survey;Guillausseau;Ann Intern Med,2001

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