Association of Novel POLGMutations and Multiple Mitochondrial DNA Deletions With Variable Clinical Phenotypes in a Spanish Population-Reference-Cited by-同舟云学术

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Association of Novel POLGMutations and Multiple Mitochondrial DNA Deletions With Variable Clinical Phenotypes in a Spanish Population

Published:2006-01-01 Issue:1 Volume:63 Page:107
ISSN:0003-9942
Container-title:Archives of Neurology
language:en
Short-container-title:Arch Neurol

Author:

González-Vioque Emiliano,Blázquez Alberto,Fernández-Moreira Daniel,Bornstein Belén,Bautista Juan,Arpa Javier,Navarro Carmen,Campos Yolanda,Fernández-Moreno Miguel A.,Garesse Rafael,Arenas Joaquin,Martín Miguel A.

Publisher

American Medical Association (AMA)

Subject

Neurology (clinical),Arts and Humanities (miscellaneous)

Cited by 56 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. Polγ coordinates DNA synthesis and proofreading to ensure mitochondrial genome integrity;Nature Structural & Molecular Biology;2023-05-18

2. The impact of mitochondria-related POLG and TFAM variants on breast cancer pathomorphological characteristics and patient outcomes;Biomarkers;2021-03-26

3. Expanding the genotype–phenotype correlation of childhood sensory polyneuropathy of genetic origin;Scientific Reports;2020-09-30

4. Modeling of pathogenic variants of mitochondrial DNA polymerase: insight into the replication defects and implication for human disease;Biochimica et Biophysica Acta (BBA) - General Subjects;2020-07

5. Progressive external ophthalmoplegia;Russian neurological journal;2020-01-29

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