(Q44338449)

2 December 2017

title

Molecular epidemiology of mtDNA mutations in 903 Chinese families suspected with Leber hereditary optic neuropathy (English)

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2 December 2017

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Xiaoyun Jia

1

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2 December 2017

Shiqiang Li

2

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2 December 2017

Xueshan Xiao

3

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2 December 2017

Xiangming Guo

4

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2 December 2017

Qingjiong Zhang

5

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2 December 2017

publication date

14 September 2006

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Journal of Human Genetics

2 December 2017

published in

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2 December 2017

volume

51

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2 December 2017

issue

10

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2 December 2017

page(s)

851-856

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An ND-6 mitochondrial DNA mutation associated with Leber hereditary optic neuropathy

2 December 2017

cites work

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12 December 2020

Diagnostic screening of mitochondrial DNA mutations in Australian adults 1990-2001.

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12 December 2020

Features of mtDNA mutation patterns in European pedigrees and sporadic cases with Leber hereditary optic neuropathy.

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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

Screening for the two most frequent mutations in Leber's hereditary optic neuropathy by duplex PCR based on allele-specific amplification

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12 December 2020

Molecular genetic basis of primary inherited optic neuropathies.

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12 December 2020

Spectrum of pathogenic mitochondrial DNA mutations and clinical features in Japanese families with Leber's hereditary optic neuropathy

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12 December 2020

Frequency of rare mitochondrial DNA mutations in patients with suspected Leber's hereditary optic neuropathy

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12 December 2020

Primary pathogenic mtDNA mutations in multigeneration pedigrees with Leber hereditary optic neuropathy.

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12 December 2020

Leber′s Hereditary Optic Neuropathy (LHON)-Related Mitochondrial DNA Sequence Changes in Italian Patients Presenting with Sporadic Bilateral Optic Neuritis

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12 December 2020

Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy

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12 December 2020

Spectrum of the mitochondrial DNA mutations of Leber's hereditary optic neuropathy in Koreans.

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12 December 2020

Differential occurrence of mutations causative of eye diseases in the Chinese population

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12 December 2020

Screening for mt-DNA mutations in optic neuritis of unknown cause

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12 December 2020

The epidemiology of Leber hereditary optic neuropathy in the North East of England

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12 December 2020

Leber's hereditary optic neuropathy with 14484 mutation in Central Java, Indonesia.

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12 December 2020

Molecular analysis for mitochondrial DNA disorders

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12 December 2020

Leber's hereditary optic neuropathy--the spectrum of mitochondrial DNA mutations in Chinese patients

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12 December 2020

Leber's hereditary optic neuropathy in Thailand

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12 December 2020

Mutation detection in Leber's hereditary optic neuropathy by PCR with allele-specific priming

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12 December 2020

De novo COX2 mutation in a LHON family of Caucasian origin: implication for the role of mtDNA polymorphism in human pathology

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12 December 2020

A new mtDNA mutation associated with Leber hereditary optic neuroretinopathy

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12 December 2020

Rapid and sensitive detection of point mutations and DNA polymorphisms using the polymerase chain reaction

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12 December 2020

The unique characteristics of Thai Leber hereditary optic neuropathy: analysis of 30 G11778A pedigrees

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12 December 2020

Exclusive homoplasmic 11778 mutation in mitochondrial DNA of Chinese patients with Leber's hereditary optic neuropathy

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12 December 2020

Molecular genetic analysis of a sporadic case of Leber hereditary optic neuropathy

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12 December 2020

Sporadic Leber hereditary optic neuropathy in Australia and New Zealand

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12 December 2020

[DNA diagnosis of Leber's hereditary optic neuropathy performed at Keio University Hospital]

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12 December 2020

10.1007/S10038-006-0032-2

Identifiers

DOI

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2 December 2017

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