Mitochondrial DNA variant 11719G is a marker for the mtDNA haplogroup cluster HV

Human Biology

Volumn 72, Issue 6, 2000, Pages 1065-1068

  Saillard, J ^a   Magalhaes P J ^a   Schwartz, M ^a   Rosenberg, T ^a   Norby S ^a  

^a UNIVERSITY OF COPENHAGEN   (Denmark)

Author keywords

MTDNA haplogroups; MTDNA polymorphisms; NP 11719; Population genetics

Indexed keywords

ALLELE; DNA POLYMORPHISM; EUROPE; GENE CLUSTER; GENETIC CORRELATION; HUMAN GENE; MITOCHONDRIAL DNA; POLYMERASE CHAIN REACTION; RESTRICTION FRAGMENT LENGTH POLYMORPHISM;

DENMARK; DNA, MITOCHONDRIAL; GENETIC MARKERS; HAPLOTYPES; HUMANS; OPTIC ATROPHIES, HEREDITARY; POLYMORPHISM, GENETIC;

EID: 0034477308     PISSN: 00187143     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (11)

1. Sequence and organization of the human mitochondrial genome
2. Reanalysis and revision of the Cambridge reference sequence for human mitochondrial DNA
3. Leber's hereditary optic neuropathy: A model for mitochondrial neurodegenerative diseases
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5. The sequence of human mtDNA: The question of errors versus polymorphisms
6. The emerging tree of west Eurasian mtDNAs: A synthesis of control-region sequences and RFLPs
7. The spectrum of pathogenic mutations and mtDNA haplogroups among Danish lineages manifesting Leber hereditary optic neuropathy
8. MtDNA analysis reveals a major late paleolithic population expansion from southwestern to northeastern Europe