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

Author:

Tabebi Mouna12ORCID,Safi Wajdi3,Felhi Rahma1,Alila Fersi Olfa1,Keskes Leila2ORCID,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

Reference54 articles.

1. Whole mitochondrial genome analysis in two families with dilated mitochondrial cardiomyopathy: detection of mutations in MT-ND2 and MT-TL1 genes

2. Maternally transmitted diabetes and deafness associated with a 10.4 kb mitochondrial DNA deletion

3. Surveyor™ Nuclease: A new strategy for a rapid identification of heteroplasmic mitochondrial DNA mutations in patients with respiratory chain defects

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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