Mitochondrial tRNA mutations and disease
Author:
Affiliation:
1. Mitochondrial Research Group, Institute for Ageing and Health, The Medical School, Newcastle University, Newcastle upon Tyne, NE2 4HH, UK
Publisher
Wiley
Subject
Molecular Biology,Biochemistry
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/wrna.27
Reference146 articles.
1. The MitoMAP database an online compendium of human mitochondrial DNA variation can be accessed athttp://www.mitomap.org/MITOMAPThe Mamit‐tRNA database (http://mamit‐trna.u‐strasbg.fr/) provides information on mammalian tRNA sequences and 2‐D structures as well as details of human mt‐tRNA mutations linked with disease.
2. Mitochondrial DNA mutations in human disease
3. Mitochondrial disorders
4. A reduction of mitochondrial DNA molecules during embryogenesis explains the rapid segregation of genotypes
5. Purifying selection of mtDNA and its implications for understanding evolution and mitochondrial disease
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