An integrated approach for classifying mitochondrial DNA variants: one clinical diagnostic laboratory’s experience
Author:
Publisher
Elsevier BV
Subject
Genetics (clinical)
Link
http://www.nature.com/articles/gim20124.pdf
Reference20 articles.
Cited by 39 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. Spectrum of germline and somatic mitochondrial DNA variants in Tuberous Sclerosis Complex;Frontiers in Genetics;2023-01-30
2. Implications of mitochondrial DNA variants in pediatric B-cell acute lymphoblastic leukemia;Egyptian Journal of Medical Human Genetics;2022-08-30
3. Phenotype-Genotype Analysis Based on Molecular Classification in 135 Children With Mitochondrial Disease;Pediatric Neurology;2022-07
4. Analysis of the entire mitochondrial genome reveals Leber’s hereditary optic neuropathy mitochondrial DNA mutations in an Arab cohort with multiple sclerosis;Scientific Reports;2022-06-30
5. Genomic Landscape of the Mitochondrial Genome in the United Arab Emirates Native Population;Genes;2020-08-01
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