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

BACKGROUND: Mitochondrial diabetes is a kind of rare diabetes caused by monogenic mutation in mitochondia. The study aimed to summarize the clinical phenotype profiles in mitochondrial diabetes withm.3243A>G mitochondrial DNA mutation and to investigate the mechanism in this kind of diabetes by a...

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Detalles Bibliográficos
Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4599722/
https://www.ncbi.nlm.nih.gov/pubmed/26449496
http://dx.doi.org/10.1186/s12881-015-0238-2

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4599722/
https://www.ncbi.nlm.nih.gov/pubmed/26449496
http://dx.doi.org/10.1186/s12881-015-0238-2

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