A specific point mutation in the mitochondrial genome of Caucasians with MELAS-Reference-Cited by-同舟云学术

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A specific point mutation in the mitochondrial genome of Caucasians with MELAS

Published:1991-12 Issue:2 Volume:88 Page:
ISSN:0340-6717
Container-title:Human Genetics
language:en
Short-container-title:Hum Genet

Author:

Enter C.,M�ller-H�cker J.,Zierz S.,Kurlemann G.,Pongratz D.,F�rster C.,Obermaier-Kusser B.,Gerbitz K.-D.

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1007/BF00206080.pdf

Cited by 25 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. Negative correlation between organ heteroplasmy, particularly hepatic heteroplasmy, and age at death revealed by post-mortem studies of m.3243A > G cases;Molecular Genetics and Metabolism;2023-11

2. Commentary: The mutations and clinical variability in maternally inherited diabetes and deafness: an analysis of 161 patients;Frontiers in Endocrinology;2023-06-07

3. Comprehensive summary of mitochondrial DNA alterations in the postmortem human brain: A systematic review;eBioMedicine;2022-02

4. Heteroplasmy and Copy Number in the Common m.3243A>G Mutation—A Post-Mortem Genotype–Phenotype Analysis;Genes;2020-02-18

5. Molecular basis of stroke;Clinical Molecular Medicine;2020

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