(Q43639975)

25 November 2017

title

Quantitation of heteroplasmy in mitochondrial DNA mutations by primer extension using Vent(R)(exo-) DNA polymerase and RFLP analysis (English)

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25 November 2017

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Jacobi FK

1

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25 November 2017

Meyer J

series ordinal

2

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25 November 2017

Pusch CM

series ordinal

3

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25 November 2017

Wissinger B

series ordinal

4

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25 November 2017

language of work or name

English

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publication date

1 July 2001

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25 November 2017

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25 November 2017

volume

478

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25 November 2017

issue

1-2

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25 November 2017

page(s)

141-151

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Rapid evolution of animal mitochondrial DNA

25 November 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0027-5107%2801%2900134-8

Clonal expansion of mitochondrial DNA with multiple deletions in autosomal dominant progressive external ophthalmoplegia

7 January 2021

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https://api.crossref.org/works/10.1016%2FS0027-5107%2801%2900134-8

Molecular genetic aspects of human mitochondrial disorders

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0027-5107%2801%2900134-8

Genetic heterogeneity and mitochondrial DNA heteroplasmy in Leber's hereditary optic neuropathy.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0027-5107%2801%2900134-8

Heteroplasmy in Leber's hereditary optic neuropathy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0027-5107%2801%2900134-8

Quantitation of heteroplasmy of mitochondrial tRNA(Leu(UUR)) gene using PCR-SSCP

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0027-5107%2801%2900134-8

Multiplex fluorescence-based primer extension method for quantitative mutation analysis of mitochondrial DNA and its diagnostic application for Alzheimer's disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0027-5107%2801%2900134-8

Quantification of point mutations associated with Leber hereditary optic neuroretinopathy by solid-phase minisequencing

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0027-5107%2801%2900134-8

Level of heteroplasmy for the mitochondrial mutation A3243G correlates with age at onset of diabetes and deafness

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0027-5107%2801%2900134-8

Marked replicative advantage of human mtDNA carrying a point mutation that causes the MELAS encephalomyopathy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0027-5107%2801%2900134-8

Quantitation of mitochondrial DNA carrying tRNALys mutation in MERRF patients

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0027-5107%2801%2900134-8

A simple salting out procedure for extracting DNA from human nucleated cells

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0027-5107%2801%2900134-8

Oxidative phosphorylation defects and Alzheimer's disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0027-5107%2801%2900134-8

Mitochondrial medicine--recent advances

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0027-5107%2801%2900134-8

Genetics of male infertility

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0027-5107%2801%2900134-8

10.1016/S0027-5107(01)00134-8

7 January 2021

Identifiers

DOI

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25 November 2017

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