A Tunisian patient with Pearson syndrome harboring the 4.977 kb common deletion associated to two novel large-scale mitochondrial deletions-Reference-Cited by-同舟云学术

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A Tunisian patient with Pearson syndrome harboring the 4.977 kb common deletion associated to two novel large-scale mitochondrial deletions

Published:2011-07 Issue:2 Volume:411 Page:381-386
ISSN:0006-291X
Container-title:Biochemical and Biophysical Research Communications
language:en
Short-container-title:Biochemical and Biophysical Research Communications

Author:

Ayed Imen Ben,Chamkha Imen,Mkaouar-Rebai Emna,Kammoun Thouraya,Mezghani Najla,Chabchoub Imen,Aloulou Hajer,Hachicha Mongia,Fakhfakh Faiza

Funder

Ministère de l’Enseignement Supérieur et de la Recherche Scientifique

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Biochemistry,Biophysics

Reference37 articles.

1. Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathies;Holt;Nature,1988

2. Mitochondrial DNA deletions in progressive external ophthalmoplegia and Kearns–Sayre syndrome;Moraes;N. Engl. J. Med.,1989

3. Deletions of mitochondrial DNA in Kearns–Sayre syndrome;Zeviani;Neurology,1988

4. Mitochondrial DNA deletion in Pearson’s marrow/pancreas syndrome;Rotig;Lancet i,1989

5. Spectrum of mitochondrial DNA rearrangements in the Pearson marrow–pancreas syndrome;Rotig;Hum. Mol. Genet.,1995

Cited by 5 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Thermodynamic analysis of DNA hybridization signatures near mitochondrial DNA deletion breakpoints;iScience;2021-03

2. Pearson Syndrome: A Rare Cause of Failure to Thrive in Infants;Clinical Pediatrics;2019-03-07

3. A novel mitochondrial DNA deletion in a patient with Pearson syndrome and neonatal diabetes mellitus provides insight into disease etiology, severity and progression;Mitochondrial DNA Part A;2015-05-27

4. Novel 5.712 kb mitochondrial DNA deletion in a patient with Pearson syndrome: A case report;Molecular Medicine Reports;2014-12-22

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

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