A whole mitochondrial genome screening in a MELAS patient: A novel mitochondrial tRNAVal mutation-Reference-Cited by-同舟云学术

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A whole mitochondrial genome screening in a MELAS patient: A novel mitochondrial tRNAVal mutation

Published:2011-04 Issue:4 Volume:407 Page:747-752
ISSN:0006-291X
Container-title:Biochemical and Biophysical Research Communications
language:en
Short-container-title:Biochemical and Biophysical Research Communications

Author:

Mezghani Najla,Mnif Mouna,Kacem Maha,Mkaouar-Rebai Emna,Hadj Salem Ikhlass,Kallel Nozha,charfi Nadia,Abid Mohamed,fakhfakh Faiza

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Biochemistry,Biophysics

Reference33 articles.

1. Prevalence of mitochondrial DNA disease in adults;Schaefer;Ann. Neurol.,2008

2. Pathogenic mitochondrial DNA mutations in proteincoding genes;Wong;Muscle Nerve.,2007

3. Mitochondrial cytopathies;Schmiedel;J. Neurol.,2003

4. Mutational analysis of whole mitochondrial DNA in patients with MELAS and MERRF diseases;Choi;Exp. Mol. Med.,2010

5. Mitochondrial Respiratory-chain diseases;DiMauro;N. Engl. J. Med.,2003

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1. A comprehensive review on pharmacological applications and drug-induced toxicity of valproic acid;Saudi Pharmaceutical Journal;2023-02

2. The first concurrent detection of mitochondrial DNA m.3243A>G mutation, deletion, and depletion in a family with mitochondrial diabetes;Molecular Genetics & Genomic Medicine;2020-05-11

3. Mutations that affect mitochondrial functions and their association with neurodegenerative diseases;Mutation Research/Reviews in Mutation Research;2014-01

4. Adverse drug reactions induced by valproic acid;Clinical Biochemistry;2013-10

5. Screening of mitochondrial mutations in Tunisian patients with mitochondrial disorders: An overview study;Mitochondrial DNA;2013-01-09

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