Analysis of association among clinical features and shorter leukocyte telomere length in mitochondrial diabetes with m.3243A>G mitochondrial DNA mutation-Reference-Cited by-同舟云学术

Analysis of association among clinical features and shorter leukocyte telomere length in mitochondrial diabetes with m.3243A>G mitochondrial DNA mutation

Published:2015-10-08 Issue:1 Volume:16 Page:
ISSN:1471-2350
Container-title:BMC Medical Genetics
language:en
Short-container-title:BMC Med Genet

Author:

Zhou Mei-Cen,Min Rui,Ji Jian-Jun,Zhang Shi,Tong An-Li,Xu Jian-ping,Li Zeng-Yi,Zhang Hua-Bing,Li Yu-Xiu

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1186/s12881-015-0238-2.pdf

Reference26 articles.

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3. Verma A, Moraes C, Shebert R, Bradley W. A MERRF/PEO overlap syndrome associated with the mitochondrial DNA 3243 mutation. Neurology. 1996;46:1334–6.

4. Van den Ouweland J, Lemkes H, Ruitenbeek W, Sandkujl L, de Vijlder M, Struyvenberg P, et al. Mutation in mitochondrial tRNA Leu(UUR) gene in a large pedigree with maternally transmitted Type 2 diabetes and deafness. Nat Genet. 1992;1:368–71.

5. Naing A, Kenchaiah M, Krishnan B, Mir F, Charnley A, Egan C, et al. Maternally inherited diabetes and deafness (MIDD): Diagnosis and management. J Diabetes Complications. 2014;28(4):542–6.

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