(Q42491866)

1 November 2017

title

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

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1 November 2017

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2

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1 November 2017

Yong-Gang Yao

1

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Claudio M. Bravi

series ordinal

3

object named as

Claudio M Bravi

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1 November 2017

4

Hans-Jürgen Bandelt

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1 November 2017

publication date

10 March 2006

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1 November 2017

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1 November 2017

volume

119

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1 November 2017

issue

5

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1 November 2017

page(s)

505-515

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Clinical and molecular characterization of a Chinese patient with auditory neuropathy associated with mitochondrial 12S rRNA T1095C mutation.

1 November 2017

cites work

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Crossref

https://api.crossref.org/works/10.1007%2FS00439-006-0154-9

Artificial recombination in forensic mtDNA population databases.

21 January 2018

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12 December 2020

Commentary to mitDNA research for the pathogenesis of mitochondrial disorders

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12 December 2020

Problems in FBI mtDNA database

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12 December 2020

Phantom mutation hotspots in human mitochondrial DNA.

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12 December 2020

Sequence and organization of the human mitochondrial genome

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12 December 2020

Phylogeographic analysis of mitochondrial DNA haplogroup F2 in China reveals T12338C in the initiation codon of the ND5 gene not to be pathogenic.

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12 December 2020

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

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12 December 2020

The Emerging Limbs and Twigs of the East Asian mtDNA Tree

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12 December 2020

Mitochondrial DNA sequence polymorphisms of five ethnic populations from northern China

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12 December 2020

Sequence variation in mitochondrial complex I genes: mutation or polymorphism?

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12 December 2020

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12 December 2020

Sequence polymorphisms of the mitochondrial DNA control region in 105 Chinese Han population.

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12 December 2020

Mitochondrial DNA haplogroup distribution within Leber hereditary optic neuropathy pedigrees

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12 December 2020

Clinical evaluation and sequence analysis of the complete mitochondrial genome of three Chinese patients with hearing impairment associated with the 12S rRNA T1095C mutation

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12 December 2020

Mitochondrial genome variation in eastern Asia and the peopling of Japan

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12 December 2020

Quality assessment of DNA sequence data: autopsy of a mis-sequenced mtDNA population sample.

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12 December 2020

Biochemical characterization of the mitochondrial tRNASer(UCN) T7511C mutation associated with nonsyndromic deafness

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12 December 2020

Phylogeny of east Asian mitochondrial DNA lineages inferred from complete sequences

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12 December 2020

A novel mitochondrial 12SrRNA point mutation in parkinsonism, deafness, and neuropathy

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12 December 2020

Clustering of Caucasian Leber hereditary optic neuropathy patients containing the 11778 or 14484 mutations on an mtDNA lineage.

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12 December 2020

Multiple origins of a mitochondrial mutation conferring deafness.

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12 December 2020

The African diaspora: mitochondrial DNA and the Atlantic slave trade

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12 December 2020

mtDNA variation in the South African Kung and Khwe-and their genetic relationships to other African populations.

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12 December 2020

Mitochondrial genome variation and the origin of modern humans

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12 December 2020

Phylogeny of mitochondrial DNA macrohaplogroup N in India, based on complete sequencing: implications for the peopling of South Asia

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12 December 2020

To trust or not to trust an idiosyncratic mitochondrial data set.

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12 December 2020

Mitochondrial DNA 5178A polymorphism and longevity

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12 December 2020

Clinical evaluation and mitochondrial DNA sequence analysis in three Chinese families with Leber's hereditary optic neuropathy

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12 December 2020

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.

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12 December 2020

A call for mtDNA data quality control in forensic science

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12 December 2020

Maternally inherited deafness associated with a T1095C mutation in the mDNA.

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12 December 2020

Haplotype diversity in mitochondrial DNA hypervariable region I, II and III in a Korean ethnic group from northeast China

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12 December 2020

Familial progressive sensorineural deafness is mainly due to the mtDNA A1555G mutation and is enhanced by treatment of aminoglycosides

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12 December 2020

Phylogenetic analysis of the mitochondrial genomes from Leber hereditary optic neuropathy pedigrees

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12 December 2020

A practical guide to mitochondrial DNA error prevention in clinical, forensic, and population genetics

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12 December 2020

Phylogenetic analysis of Leber's hereditary optic neuropathy mitochondrial DNA's indicates multiple independent occurrences of the common mutations

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12 December 2020

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12 December 2020

Disuniting uniformity: a pied cladistic canvas of mtDNA haplogroup H in Eurasia

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12 December 2020

Mitochondrial genes and schizophrenia

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12 December 2020

The A1555G mutation in the 12S rRNA gene of human mtDNA: recurrent origins and founder events in families affected by sensorineural deafness

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12 December 2020

In search of geographical patterns in European mitochondrial DNA.

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12 December 2020

A critical reassessment of the role of mitochondria in tumorigenesis

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12 December 2020

Cosegregation of the G7444A mutation in the mitochondrial COI/tRNA(Ser(UCN)) genes with the 12S rRNA A1555G mutation in a Chinese family with aminoglycoside-induced and nonsyndromic hearing loss

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12 December 2020

Phylogeographic differentiation of mitochondrial DNA in Han Chinese

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12 December 2020

Phylogenetic network for European mtDNA.

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12 December 2020

Only male matrilineal relatives with Leber's hereditary optic neuropathy in a large Chinese family carrying the mitochondrial DNA G11778A mutation

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12 December 2020

Mitochondrial DNA control region sequences in Koreans: identification of useful variable sites and phylogenetic analysis for mtDNA data quality control.

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12 December 2020

About the "Pathological" role of the mtDNA T3308C mutationellipsis

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12 December 2020

Proving pathogenicity: when evolution is not enough

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12 December 2020

Detecting errors in mtDNA data by phylogenetic analysis

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12 December 2020

Extremely low penetrance of hearing loss in four Chinese families with the mitochondrial 12S rRNA A1555G mutation

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12 December 2020

Haplogroup effects and recombination of mitochondrial DNA: novel clues from the analysis of Leber hereditary optic neuropathy pedigrees.

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12 December 2020

Identification of Native American founder mtDNAs through the analysis of complete mtDNA sequences: some caveats.

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12 December 2020

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

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12 December 2020

Diabetes mellitus: a "thrifty" genotype rendered detrimental by "progress"?

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12 December 2020

Maternally inherited aminoglycoside-induced and nonsyndromic deafness is associated with the novel C1494T mutation in the mitochondrial 12S rRNA gene in a large Chinese family

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12 December 2020

Low "penetrance" of phylogenetic knowledge in mitochondrial disease studies

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12 December 2020

Reduced-median-network analysis of complete mitochondrial DNA coding-region sequences for the major African, Asian, and European haplogroups

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12 December 2020

Different matrilineal contributions to genetic structure of ethnic groups in the silk road region in china

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12 December 2020

Reanalysis and revision of the Cambridge reference sequence for human mitochondrial DNA

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12 December 2020

More evidence for non-maternal inheritance of mitochondrial DNA?

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12 December 2020

A new database of mitochondrial DNA hypervariable regions I and II sequences from 162 Japanese individuals

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12 December 2020

An annotated mtDNA database

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12 December 2020

Sequence analysis of the complete mitochondrial genome in patients with mitochondrial encephaloneuromyopathies lacking the common pathogenic DNA mutations.

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12 December 2020

The fingerprint of phantom mutations in mitochondrial DNA data

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12 December 2020

The making of the African mtDNA landscape

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12 December 2020

Mosaics of ancient mitochondrial DNA: positive indicators of nonauthenticity

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12 December 2020

Mutational analysis of the mitochondrial 12S rRNA gene in Chinese pediatric subjects with aminoglycoside-induced and non-syndromic hearing loss

1 reference

12 December 2020

Phylogenetic analysis of mitochondrial DNA in Japanese pedigrees of sensorineural hearing loss associated with the A1555G mutation

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12 December 2020

Forensic genetic analysis of mitochondrial DNA hypervariable region I/II sequences: an expanded Korean population database

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12 December 2020

Cosegregation of C-insertion at position 961 with the A1555G mutation of the mitochondrial 12S rRNA gene in a large Chinese family with maternally inherited hearing loss

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12 December 2020

Reconstructing the evolutionary history of China: a caveat about inferences drawn from ancient DNA

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12 December 2020

Maternally inherited nonsyndromic hearing loss is associated with the T7511C mutation in the mitochondrial tRNASerUCN gene in a Japanese family

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12 December 2020

The role of selection in the evolution of human mitochondrial genomes

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12 December 2020

10.1007/S00439-006-0154-9

Identifiers

DOI

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Dimensions Publication ID

1 November 2017

1018484485

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