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Mitochondrial DNA
The Journal of DNA Mapping, Sequencing, and Analysis
Volume 24, 2013 - Issue 3
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Screening of mitochondrial mutations in Tunisian patients with mitochondrial disorders: An overview study

Emna Mkaouar-RebaiHuman Molecular Genetic Laboratory, Faculty of Medicine of Sfax, University of Sfax, Sfax, TunisiaCorrespondence[email protected] [email protected]
,
Imen ChamkhaHuman Molecular Genetic Laboratory, Faculty of Medicine of Sfax, University of Sfax, Sfax, Tunisia
,
Najla MezghaniHuman Molecular Genetic Laboratory, Faculty of Medicine of Sfax, University of Sfax, Sfax, Tunisia
,
Imen Ben AyedHuman Molecular Genetic Laboratory, Faculty of Medicine of Sfax, University of Sfax, Sfax, Tunisia
&
Faiza FakhfakhHuman Molecular Genetic Laboratory, Faculty of Medicine of Sfax, University of Sfax, Sfax, TunisiaCorrespondence[email protected] [email protected]
Pages 163-178 | Received 23 Sep 2012, Accepted 06 Nov 2012, Published online: 09 Jan 2013

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Soundarya Priya Alexandar, Indhumathi Dhinakaran, Vidhya Ravi, Nandhini Parthasarathy, Somasundari Ganesan, Muthumeenakshi Bhaskaran & Ganesh Prasad Arun Kumar. (2017) Meta-Analysis of Association of Mitochondrial DNA Mutations with Type 2 Diabetes and Gestational Diabetes Mellitus. International Journal of Human Genetics 17:4, pages 177-190.
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Yasemin Gulcan Kurt, Emin Ozgur Akgul & Tuncer Caycı. (2014) MtDNA depletions are also one of major cause of mitochondrial disease. Mitochondrial DNA 25:4, pages 303-303.
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Articles from other publishers (6)

Yanqin Ying, Yan Liang, Xiaoping Luo & Ming Wei. (2022) Case Report: Clinical and Genetic Characteristics of Pearson Syndrome in a Chinese Boy and 139 Patients. Frontiers in Genetics 13.
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Samuel Mawuli Adadey, Edmond Wonkam-Tingang, Elvis Twumasi Aboagye, Osbourne Quaye, Gordon A. Awandare & Ambroise Wonkam. (2021) Hearing loss in Africa: current genetic profile. Human Genetics 141:3-4, pages 505-517.
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Nessrine Mezzi, Olfa Messaoud, Rahma Mkaouar, Nadia Zitouna, Safa Romdhane, Ghaith Abdessalem, Cherine Charfeddine, Faouzi Maazoul, Ines Ouerteni, Yosr Hamdi, Anissa Zaouak, Ridha Mrad, Sonia Abdelhak & Lilia Romdhane. (2021) Spectrum of Genetic Diseases in Tunisia: Current Situation and Main Milestones Achieved. Genes 12:11, pages 1820.
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Mohaddeseh Behjati, Mohammad Reza Sabri, Masood Etemadi Far & Majid Nejati. (2020) Cardiac complications in inherited mitochondrial diseases. Heart Failure Reviews 26:2, pages 391-403.
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Josef Finsterer & Sonam Kothari. (2014) Cardiac manifestations of primary mitochondrial disorders. International Journal of Cardiology 177:3, pages 754-763.
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Varinderpal S. Dhillon & Michael Fenech. (2014) Mutations that affect mitochondrial functions and their association with neurodegenerative diseases. Mutation Research/Reviews in Mutation Research 759, pages 1-13.
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