about
Major genomic mitochondrial lineages delineate early human expansionsMolecular instability in the COII-tRNA(Lys) intergenic region of the human mitochondrial genome: multiple origins of the 9-bp deletion and heteroplasmy for expanded repeats.Haplotype and phylogenetic analyses suggest that one European-specific mtDNA background plays a role in the expression of Leber hereditary optic neuropathy by increasing the penetrance of the primary mutations 11778 and 14484.Mutational analysis of the mitochondrial tRNA genes and flanking regions in umbilical cord tissue from uninfected infants receiving AZT-based therapies for prophylaxis of HIV-1.mtDNA control-region sequence variation suggests multiple independent origins of an "Asian-specific" 9-bp deletion in sub-Saharan Africans.
P2860
description
1995 nî lūn-bûn
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1995年の論文
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1995年論文
@yue
1995年論文
@zh-hant
1995年論文
@zh-hk
1995年論文
@zh-mo
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@zh-tw
1995年论文
@wuu
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name
About the "Asian"-specific 9-bp deletion of mtDNA....
@en
About the "Asian"-specific 9-bp deletion of mtDNA....
@nl
type
label
About the "Asian"-specific 9-bp deletion of mtDNA....
@en
About the "Asian"-specific 9-bp deletion of mtDNA....
@nl
prefLabel
About the "Asian"-specific 9-bp deletion of mtDNA....
@en
About the "Asian"-specific 9-bp deletion of mtDNA....
@nl
P2093
P2860
P1476
About the "Asian"-specific 9-bp deletion of mtDNA....
@en
P2093
D Sellitto
F Cruciani
M Petrozzi
P Santolamazza
R Scozzari
P2860
P304
P407
P577
1995-08-01T00:00:00Z