Mitochondrial DNA haplogroups do not play a role in the variable phenotypic presentation of the A3243G mutation.
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Phylogeny of east Asian mitochondrial DNA lineages inferred from complete sequencesGenetic, pathogenetic, and phenotypic implications of the mitochondrial A3243G tRNALeu(UUR) mutationFrequency of mitochondrial mutations in non-syndromic hearing loss as well as possibly responsible variants found by whole mitochondrial genome screeningNon-syndromic Hearing Impairment in a Hungarian Family with the m.7510T>C Mutation of Mitochondrial tRNA(Ser(UCN)) and Review of Published Cases.A six-generation Chinese family in haplogroup B4C1C exhibits high penetrance of 1555A > G-induced hearing LossNew evidence of a mitochondrial genetic background paradox: impact of the J haplogroup on the A3243G mutation.Systematic analysis of mitochondrial genes associated with hearing loss in the Japanese population: dHPLC reveals a new candidate mutationThe case for the continuing use of the revised Cambridge Reference Sequence (rCRS) and the standardization of notation in human mitochondrial DNA studies.Haplogroup effects and recombination of mitochondrial DNA: novel clues from the analysis of Leber hereditary optic neuropathy pedigrees.Molecular mechanisms of mitochondrial diabetes (MIDD).Mitochondrial DNA and disease.Clinical and Molecular Characteristics in 100 Chinese Pediatric Patients with m.3243A>G Mutation in Mitochondrial DNASingle-cell A3243G mitochondrial DNA mutation load assays for segregation analysisAssociating mitochondrial DNA variation with complex traits.Mitochondrial DNA mutations in patients with postlingual, nonsyndromic hearing impairment.Novel mutations m.3959G>A and m.3995A>G in mitochondrial gene MT-ND1 associated with MELAS.Prevalence of mitochondrial DNA haplogroups in an Australian population.Background sequence characteristics influence the occurrence and severity of disease-causing mtDNA mutations.Analysis of complete mitochondrial genomes of patients with schizophrenia and bipolar disordermtDNA Population Variants and Neurodegenerative DiseasesMitochondrial Genomics: A complex field now coming of age
P2860
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P2860
Mitochondrial DNA haplogroups do not play a role in the variable phenotypic presentation of the A3243G mutation.
description
2003 nî lūn-bûn
@nan
2003 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
2003 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
2003年の論文
@ja
2003年論文
@yue
2003年論文
@zh-hant
2003年論文
@zh-hk
2003年論文
@zh-mo
2003年論文
@zh-tw
2003年论文
@wuu
name
Mitochondrial DNA haplogroups ...... tation of the A3243G mutation.
@ast
Mitochondrial DNA haplogroups ...... tation of the A3243G mutation.
@en
type
label
Mitochondrial DNA haplogroups ...... tation of the A3243G mutation.
@ast
Mitochondrial DNA haplogroups ...... tation of the A3243G mutation.
@en
prefLabel
Mitochondrial DNA haplogroups ...... tation of the A3243G mutation.
@ast
Mitochondrial DNA haplogroups ...... tation of the A3243G mutation.
@en
P2093
P2860
P50
P356
P1476
Mitochondrial DNA haplogroups ...... tation of the A3243G mutation.
@en
P2093
Alberto García
Antonio Torroni
Chiara Rengo
Daniele Sellitto
Pilar Jara
Rosaria Scozzari
Yolanda Campos
P2860
P304
P356
10.1086/373936
P407
P577
2003-02-24T00:00:00Z