Molecular investigations of mitochondrial deletions: Evaluating the usefulness of different genetic tests-Reference-Cited by-同舟云学术

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Molecular investigations of mitochondrial deletions: Evaluating the usefulness of different genetic tests

Published:2012-09 Issue:1 Volume:506 Page:161-165
ISSN:0378-1119
Container-title:Gene
language:en
Short-container-title:Gene

Author:

Tońska Katarzyna,Piekutowska-Abramczuk Dorota,Kaliszewska Magdalena,Kowalski Paweł,Tańska Anna,Bartnik Ewa,Pronicka Ewa,Krajewska-Walasek Małgorzata

Funder

CMHI Project

National Science Centre Projects

Publisher

Elsevier BV

Subject

Genetics,General Medicine

Reference20 articles.

1. Multiple deletions of mtDNA remove the light strand origin of replication;Bank;Biochem. Biophys. Res. Commun.,2000

2. Cellular and molecular studies in muscle and cultures from patients with multiple mitochondrial DNA deletions;Carrozzo;J. Neurol. Sci.,1999

3. The generation of mitochondrial DNA large-scale deletions in human cells;Chen;J. Hum. Genet.,2011

4. The epidemiology of pathogenic mitochondrial DNA mutations;Chinnery;Ann. Neurol.,2000

5. Risk of developing a mitochondrial DNA deletion disorder;Chinnery;Lancet,2004

Cited by 8 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. Cellular and Molecular Responses to Mitochondrial DNA Deletions in Kearns-Sayre Syndrome: Some Underlying Mechanisms;Molecular Neurobiology;2024-01-15

2. Kearns‐Sayre syndrome case. Novel 5,9 kb mtDNA deletion;Molecular Genetics & Genomic Medicine;2022-10

3. eKLIPse: a sensitive tool for the detection and quantification of mitochondrial DNA deletions from next-generation sequencing data;Genetics in Medicine;2019-06

4. Maternally inherited Leigh syndrome detected by Multiplex ligation-dependent probe amplification;Mitochondrial DNA Part B;2019-01-02

5. Mitochondrial DNA deletions detected by Multiplex Ligation-dependent Probe Amplification;Mitochondrial DNA Part A;2015-06-26

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