Clinical and molecular characterization of mitochondrial DNA disorders in a group of Argentinian pediatric patients-Reference-Cited by-同舟云学术

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Clinical and molecular characterization of mitochondrial DNA disorders in a group of Argentinian pediatric patients

Published:2021-06 Issue: Volume:27 Page:100733
ISSN:2214-4269
Container-title:Molecular Genetics and Metabolism Reports
language:en
Short-container-title:Molecular Genetics and Metabolism Reports

Author:

Loos Mariana Amina,Gomez Gimena,Mayorga Lía,Caraballo Roberto Horacio,Eiroa Hernán Diego,Obregon María Gabriela,Rugilo Carlos,Lubieniecki Fabiana,Taratuto Ana Lía,Saccoliti María,Alonso Cristina Noemi,Aráoz Hilda Verónica

Publisher

Elsevier BV

Subject

Endocrinology,Genetics,Molecular Biology

Reference54 articles.

1. Mitochondrial disease in children;Rahman;J. Intern. Med.,2020

2. Mitochondrial disorders: prevalence, myths and advances;Thorburn;J. Inherit. Metab. Dis.,2004

3. Mitochondrial genetics;Chinnery;Br. Med. Bull.,2013

4. The clinical maze of mitochondrial neurology;DiMauro;Nat. Rev. Neurol.,2013

5. Revealing the complexity of mitochondrial DNA-related disorders;Orsucci;EBioMedicine.,2018

Cited by 3 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. Phenotyping mitochondrial DNA‐related diseases in childhood: A cohort study of 150 patients;European Journal of Neurology;2023-04-25

2. Mitochondrial DNA variants in a cohort from Argentina with suspected Leber’s hereditary optic neuropathy (LHON);PLOS ONE;2023-02-24

3. Phenotypes and genotypes of mitochondrial diseases with mtDNA variations in Chinese children: A multi-center study;Mitochondrion;2022-01

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