Screening of mitochondrial mutations and insertion–deletion polymorphism in gestational diabetes mellitus in the Asian Indian population

In this study we scrutinized the association between the A8344G/A3243G mutations and a 9-bp deletion polymorphism with gestational diabetes mellitus (GDM) in an Asian Indian population. The A3243G mutation in the mitochondrial tRNA(Leu(UUR)) causes mitochondrial encephalopathy myopathy, lactic acido...

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Detalles Bibliográficos
Autores principales: Khan, Imran Ali, Shaik, Noor Ahmad, Pasupuleti, Nagarjuna, Chava, Srinivas, Jahan, Parveen, Hasan, Qurratulain, Rao, Pragna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2015
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4423658/
https://www.ncbi.nlm.nih.gov/pubmed/25972744
http://dx.doi.org/10.1016/j.sjbs.2014.11.001

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4423658/
https://www.ncbi.nlm.nih.gov/pubmed/25972744
http://dx.doi.org/10.1016/j.sjbs.2014.11.001

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