(Q28216954)

1

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Wendy Hutchison

2

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Dominic Thyagarajan

3

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Hans-Henrik M Dahl

Journal of the Neurological Sciences

4

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language of work or name

English

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publication date

15 September 2002

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published in

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volume

201

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page(s)

39-44

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issue

1-2

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cites work

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Mapping of autosomal dominant progressive external ophthalmoplegia to a 7-cM critical region on 10q24

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Role of adenine nucleotide translocator 1 in mtDNA maintenance

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Mutation of POLG is associated with progressive external ophthalmoplegia characterized by mtDNA deletions

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Human mitochondrial DNA deletions associated with mutations in the gene encoding Twinkle, a phage T7 gene 4-like protein localized in mitochondria

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

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mtDNA deletion in a patient with symptoms of mitochondrial cytopathy but without ragged red fibers.

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The linker region between the helicase and primase domains of the bacteriophage T7 gene 4 protein is critical for hexamer formation

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An autosomal locus predisposing to deletions of mitochondrial DNA

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Autosomal dominant progressive external ophthalmoplegia with multiple deletions of mtDNA: clinical, biochemical, and molecular genetic features of the 10q-linked disease.

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A third locus predisposing to multiple deletions of mtDNA in autosomal dominant progressive external ophthalmoplegia

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