The first concurrent detection of mitochondrial DNA m.3243A>G mutation, deletion, and depletion in a family with mitochondrial diabetes-Reference-Cited by-同舟云学术

The first concurrent detection of mitochondrial DNA m.3243A>G mutation, deletion, and depletion in a family with mitochondrial diabetes

Published:2020-05-11 Issue:7 Volume:8 Page:
ISSN:2324-9269
Container-title:Molecular Genetics & Genomic Medicine
language:en
Short-container-title:Mol Genet Genomic Med

Author:

Tabebi Mouna¹²^ORCID,Safi Wajdi³,Felhi Rahma¹,Alila Fersi Olfa¹,Keskes Leila²^ORCID,Abid Mohamed³,Mnif Mouna³,Fakhfakh Faiza¹

Affiliation:

1. Molecular and Functional Genetics Laboratory Faculty of Science of Sfax University of Sfax Sfax Tunisia

2. Human Molecular Genetics Laboratory Faculty of Medicine of Sfax University of Sfax Sfax Tunisia

3. Department of Endocrinology Diabetology CHU Hedi Chaker Sfax Tunisia

Funder

The Ministry of Higher Education and Scientific Research, Tunisia

Publisher

Wiley

Subject

Genetics(clinical),Genetics,Molecular Biology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/mgg3.1292

Reference54 articles.

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4. Cardiological manifestations of mitochondrial respiratory chain disorders;Berardo A.;Acta Myologica: Myopathies and Cardiomyopathies: Official Journal of the Mediterranean Society of Myology,2011

5. A3243G mitochondrial DNA mutation in Tunisian diabetic population;Bouhaha R;Tunisian medical,2010

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