(Q44673190)

5 December 2017

Exaggerated status of "novel" and "pathogenic" mtDNA sequence variants due to inadequate database searches (English)

1 reference

5 December 2017

0 references

2

1 reference

5 December 2017

Yong-Gang Yao

4

0 references

Robert William Taylor

series ordinal

3

object named as

Robert W Taylor

1 reference

5 December 2017

1

Hans-Jürgen Bandelt

1 reference

5 December 2017

1 February 2009

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5 December 2017

1 reference

5 December 2017

30

1 reference

5 December 2017

2

1 reference

5 December 2017

191-196

1 reference

The molecular dissection of mtDNA haplogroup H confirms that the Franco-Cantabrian glacial refuge was a major source for the European gene pool

5 December 2017

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20846

Detection of unrecognized low-level mtDNA heteroplasmy may explain the variable phenotypic expressivity of apparently homoplasmic mtDNA mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20846

What is a 'novel' mtDNA mutation--and does 'novelty' really matter?

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20846

The search of 'novel' mtDNA mutations in hypertrophic cardiomyopathy: MITOMAPping as a risk factor

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20846

MITOMAP: a human mitochondrial genome database--2004 update

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20846

Phantom mutation hotspots in human mitochondrial DNA.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20846

Functional polypeptides can be synthesized from human mitochondrial transcripts lacking termination codons

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20846

Phylogeographic analysis of mitochondrial DNA in northern Asian populations

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20846

High Resolution Analysis and Phylogenetic Network Construction Using Complete mtDNA Sequences in Sardinian Genetic Isolates

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20846

Analysis of mitochondrial DNA sequences in patients with isolated or combined oxidative phosphorylation system deficiency.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20846

Mitochondrial genome variation and the origin of modern humans

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20846

Mitochondrial DNA mutations in patients with postlingual, nonsyndromic hearing impairment

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20846

Frequency of mitochondrial transfer RNA mutations and deletions in 225 patients presenting with respiratory chain deficiencies

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20846

Novel mitochondrial DNA length variants and genetic instability in a family with diabetes and deafness

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20846

The role of selection in the evolution of human mitochondrial genomes

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20846

Phylogeny of east Asian mitochondrial DNA lineages inferred from complete sequences

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20846

Major genomic mitochondrial lineages delineate early human expansions

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20846

Mitochondrial DNA variability in Slovaks, with application to the Roma origin

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20846

Natural selection shaped regional mtDNA variation in humans

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20846

The mtDNA legacy of the Levantine early Upper Palaeolithic in Africa

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20846

Patients with idiopathic cardiomyopathy belong to the same mitochondrial DNA gene family of Parkinson's disease and mitochondrial encephalomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20846

Maternal traces of deep common ancestry and asymmetric gene flow between Pygmy hunter-gatherers and Bantu-speaking farmers

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20846

Polymorphism, heteroplasmy, mitochondrial fusion and diabetes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20846

Mitochondrial DNA transfer RNA gene sequence variations in patients with mitochondrial disorders.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20846

The dazzling array of basal branches in the mtDNA macrohaplogroup M from India as inferred from complete genomes

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20846

Mitochondrial genome variation in eastern Asia and the peopling of Japan

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20846

Do the four clades of the mtDNA haplogroup L2 evolve at different rates?

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20846

Traces of archaic mitochondrial lineages persist in Austronesian-speaking Formosan populations

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20846

Sequence variation in the tRNA genes of human mitochondrial DNA.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20846

Pathogenic mitochondrial DNA mutations in protein-coding genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20846

A reappraisal of complete mtDNA variation in East Asian families with hearing impairment

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20846

Clinical evaluation and mitochondrial DNA sequence analysis in two Chinese families with aminoglycoside-induced and non-syndromic hearing loss.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20846

A novel ND3 mitochondrial DNA mutation in three Korean children with basal ganglia lesions and complex I deficiency.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20846

7 January 2021

NDUFS6 mutations are a novel cause of lethal neonatal mitochondrial complex I deficiency

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20846

7 January 2021

Identification of a mutation in the mitochondrial tRNA(Cys) gene associated with mitochondrial encephalopathy

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20846

7 January 2021

Mitochondrial tRNACys gene mutation (A5814G): a second family with mitochondrial encephalopathy

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20846

7 January 2021

A novel recurrent mitochondrial DNA mutation in ND3 gene is associated with isolated complex I deficiency causing Leigh syndrome and dystonia

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20846

7 January 2021

Exhaustive scanning approach to screen all the mitochondrial tRNA genes for mutations and its application to the investigation of 35 independent patients with mitochondrial disorders

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20846

7 January 2021

Variants in mitochondrial tRNAGlu, tRNAArg, and tRNAThr may influence the phenotypic manifestation of deafness-associated 12S rRNA A1555G mutation in three Han Chinese families with hearing loss

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20846

7 January 2021

Identifiers

DOI

10.1002/HUMU.20846

1 reference

5 December 2017

1 reference

PubMed ID

18800376