scholarly article | Q13442814 |
P50 | author | Alessandro Achilli | Q28468771 |
Antonio Salas | Q30504065 | ||
Yong-Gang Yao | Q47667115 | ||
Hans-Jürgen Bandelt | Q102165184 | ||
P2093 | author name string | Antonio Torroni | |
Ya-Ping Zhang | |||
Chang Sun | |||
Shi-Fang Wu | |||
Li Zhong | |||
Qing-Peng Kong | |||
Cheng-Ye Wang | |||
Chun-Ling Zhu | |||
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Single, Rapid Coastal Settlement of Asia Revealed by Analysis of Complete Mitochondrial Genomes | Q22065802 | ||
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Natural selection shaped regional mtDNA variation in humans | Q24541289 | ||
Mitochondrial genome variation in eastern Asia and the peopling of Japan | Q24562348 | ||
Reduced-median-network analysis of complete mitochondrial DNA coding-region sequences for the major African, Asian, and European haplogroups | Q24563892 | ||
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Phylogeographic differentiation of mitochondrial DNA in Han Chinese | Q24632824 | ||
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Reanalysis and revision of the Cambridge reference sequence for human mitochondrial DNA | Q27860870 | ||
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An ND-6 mitochondrial DNA mutation associated with Leber hereditary optic neuropathy | Q28156628 | ||
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Mitochondrial DNA sequence polymorphisms of five ethnic populations from northern China | Q28203371 | ||
Reconstructing the evolutionary history of China: a caveat about inferences drawn from ancient DNA | Q28211204 | ||
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Sequence analysis of the mitochondrial genomes from Dutch pedigrees with Leber hereditary optic neuropathy | Q33904852 | ||
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Haplogroup effects and recombination of mitochondrial DNA: novel clues from the analysis of Leber hereditary optic neuropathy pedigrees. | Q34507282 | ||
mtDNA mutations and common neurodegenerative disorders | Q36254228 | ||
Mechanism of somatic mitochondrial DNA mutations associated with age and diseases | Q40437270 | ||
Comparative analysis of the pathogenic mechanisms associated with the G8363A and A8296G mutations in the mitochondrial tRNA(Lys) gene. | Q40489976 | ||
The A8296G mtDNA mutation associated with several mitochondrial diseases does not cause mitochondrial dysfunction in cybrid cell lines. | Q40749197 | ||
Attenuation of free radical production and paracrystalline inclusions by creatine supplementation in a patient with a novel cytochrome b mutation | Q42459462 | ||
A reappraisal of complete mtDNA variation in East Asian families with hearing impairment | Q42491866 | ||
Genetic relationship of Chinese ethnic populations revealed by mtDNA sequence diversity | Q42674284 | ||
To trust or not to trust an idiosyncratic mitochondrial data set. | Q42927562 | ||
Errors, phantoms and otherwise, in human mtDNA sequences | Q42927620 | ||
'Racial' differences in genetic effects for complex diseases | Q44586727 | ||
Mitochondrial DNA 3644T-->C mutation associated with bipolar disorder | Q45144296 | ||
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A case of CPT deficiency, homoplasmic mtDNA mutation and ragged red fibers at muscle biopsy | Q46707830 | ||
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Association of the mitochondrial DNA 15497G/A polymorphism with obesity in a middle-aged and elderly Japanese population | Q47707199 | ||
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Clinical evaluation and sequence analysis of the complete mitochondrial genome of three Chinese patients with hearing impairment associated with the 12S rRNA T1095C mutation. | Q50476427 | ||
Leber's hereditary optic neuropathy: the spectrum of mitochondrial DNA mutations in Iranian patients. | Q51679328 | ||
Detection of mitochondrial DNA mutations in gestational trophoblastic disease. | Q54764043 | ||
Mitochondrial genes and schizophrenia | Q57305100 | ||
Genomic Control to the extreme | Q58047101 | ||
Mitochondrial DNA 5178A polymorphism and longevity | Q59295608 | ||
P433 | issue | 13 | |
P921 | main subject | phylogenetics | Q171184 |
P304 | page(s) | 2076-2086 | |
P577 | publication date | 2006-05-19 | |
P1433 | published in | Human Molecular Genetics | Q2720965 |
P1476 | title | Updating the East Asian mtDNA phylogeny: a prerequisite for the identification of pathogenic mutations | |
P478 | volume | 15 |
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