Phylogenetic Network of the mtDNA Haplogroup U in Northern Finland Based on Sequence Analysis of the Complete Coding Region by Conformation-Sensitive Gel Electrophoresis-Reference-Cited by-同舟云学术

Phylogenetic Network of the mtDNA Haplogroup U in Northern Finland Based on Sequence Analysis of the Complete Coding Region by Conformation-Sensitive Gel Electrophoresis

Published:2000-03 Issue:3 Volume:66 Page:1017-1026
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Finnilä Saara,Hassinen Ilmo E.,Ala-Kokko Leena,Majamaa Kari

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference33 articles.

1. Rapid detection of sequence polymorphisms in the human mitochondrial DNA control region by polymerase chain reaction and single-stranded conformation analysis in mutation detection enhancement gels;Alonso;Electrophoresis,1996

2. Sequence and organization of human mitochondrial genome;Anderson;Nature,1981

3. Comparison between the complete mitochondrial DNA sequences of Homo and the common chimpanzee based on nonchimeric sequences;Arnason;J Mol Evol,1996

4. Purification of mitochondrial DNA from human cell cultures and placenta;Ausenda;Methods Enzymol,1996

5. Mitochondrial portraits of human populations using median networks;Bandelt;Genetics,1995

Cited by 87 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. Evolution and dispersal of mitochondrial DNA haplogroup U5 in Northern Europe: insights from an unsupervised learning approach to phylogeography;BMC Genomics;2022-05-07

2. Novel non-neutral mitochondrial DNA mutations found in childhood acute lymphoblastic leukemia;Clinical Genetics;2017-12-20

3. A novel MTTT mutation m.15933G > A revealed in analysis of mitochondrial DNA in patients with suspected mitochondrial disease;BMC Medical Genetics;2017-02-10

4. Genetic aetiology of ophthalmological manifestations in children - a focus on mitochondrial disease-related symptoms;Acta Ophthalmologica;2015-10-08

5. Mutations in the two ribosomal RNA genes in mitochondrial DNA among Finnish children with hearing impairment;BMC Medical Genetics;2015-02-04