POLG1-related and other "mitochondrial Parkinsonisms": an overview. (Q37827400)

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19 January 2020

review article

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title

POLG1-related and other "mitochondrial Parkinsonisms": an overview (English)

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19 January 2020

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Elena Caldarazzo Ienco

2

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19 January 2020

Gabriele Siciliano

4

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19 January 2020

author name string

Daniele Orsucci

1

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19 January 2020

Michelangelo Mancuso

3

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19 January 2020

publication date

8 January 2011

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Journal of Molecular Neuroscience

19 January 2020

published in

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19 January 2020

volume

44

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19 January 2020

issue

1

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19 January 2020

page(s)

17-24

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Variations of the CAG trinucleotide repeat in DNA polymerase γ (POLG1) is associated with Parkinson's disease in Sweden

19 January 2020

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The DNA polymerase gamma Y955C disease variant associated with PEO and parkinsonism mediates the incorporation and translesion synthesis opposite 7,8-dihydro-8-oxo-2'-deoxyguanosine

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Mitochondrial DNA polymerase W748S mutation: a common cause of autosomal recessive ataxia with ancient European origin

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Is it ADEM, POLG, or both?

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Two novel POLG1 mutations in a patient with progressive external ophthalmoplegia, levodopa-responsive pseudo-orthostatic tremor and parkinsonism

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Parkinsonism, premature menopause, and mitochondrial DNA polymerase gamma mutations: clinical and molecular genetic study.

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Functional defects due to spacer-region mutations of human mitochondrial DNA polymerase in a family with an ataxia-myopathy syndrome

21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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OPA1 IN MULTIPLE MITOCHONDRIAL DNA DELETION DISORDERS

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POLG, but notPEO1, is a frequent cause of cerebellar ataxia in Central Europe

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12 December 2020

10.1007/S12031-010-9488-9

Identifiers

DOI

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21221844%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

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