Spontaneous event of mitochondrial DNA mutation, A3243G, found in a family of identical twins
Author:
Publisher
Informa UK Limited
Subject
Genetics,Molecular Biology
Link
http://www.tandfonline.com/doi/pdf/10.3109/19401736.2012.731402
Reference42 articles.
1. Molecular pathology of MELAS and MERRF. The relationship between mutation load and clinical phenotypes
2. Extreme variability of clinical symptoms among sibs in a MELAS family correlated with heteroplasmy for the mitochondrial A3243G mutation
3. LENGTH VARIATION AND HETEROPLASMY ARE FREQUENT IN MITOCHONDRIAL DNA FROM PARTHENOGENETIC AND BISEXUAL LIZARDS (GENUS CNEMIDOPHORUS)
4. Prevalence of Mitochondrial tRNA Gene Mutations and Their Association with Specific Clinical Phenotypes in Patients with Type 2 Diabetes Mellitus of Coimbatore
5. The A to G transition at nt 3243 of the mitochondrial tRNALeu(UUR) may cause an MERRF syndrome.
Cited by 2 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. In Utero Exposure to Air Pollutants and Mitochondrial Heteroplasmy in Neonates;Environmental Science & Technology;2022-12-14
2. De Novo Mutation of m.3243A>G together with m.16093T>C Associated with Atypical Clinical Features in a Pedigree with MIDD Syndrome;Journal of Diabetes Research;2019-04-04
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