Recurrent major depression, ataxia, and cardiomyopathy: association with a novel POLG mutation? (Q35006696)

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3 February 2020

case report

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title

Recurrent major depression, ataxia, and cardiomyopathy: association with a novel POLG mutation? (English)

1 reference

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3 February 2020

2

1 reference

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3 February 2020

author name string

Willem Ma Verhoeven

1

1 reference

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3 February 2020

Berry Ph Kremer

3

1 reference

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3 February 2020

Boudewijn Jhb de Pont

4

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3 February 2020

Carlo Lm Marcelis

5

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3 February 2020

language of work or name

English

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publication date

15 May 2011

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Neuropsychiatric Disease and Treatment

3 February 2020

published in

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3 February 2020

volume

7

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3 February 2020

page(s)

293-296

1 reference

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Creative Commons Attribution-NonCommercial 3.0 Unported

3 February 2020

copyright license

start time

1 May 2011

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

cites work

Mitochondrial dysfunction and psychiatric disorders

1 reference

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Ataxias with autosomal, X-chromosomal or maternal inheritance.

8 July 2018

1 reference

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DNA polymerase gamma and mitochondrial disease: understanding the consequence of POLG mutations.

8 July 2018

1 reference

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Molecular and clinical genetics of mitochondrial diseases due to POLG mutations

8 July 2018

1 reference

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Inherited mitochondrial diseases of DNA replication

8 July 2018

1 reference

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Psychiatric comorbidity in 36 adults with mitochondrial cytopathies.

8 July 2018

1 reference

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Mitochondrial DNA polymerase-gamma and human disease

8 July 2018

1 reference

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

8 July 2018

1 reference

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8 July 2018

1 reference

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

8 July 2018

1 reference

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The unfolding clinical spectrum of POLG mutations.

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3101889

Major depression in adolescent children consecutively diagnosed with mitochondrial disorder

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3101889

Abundance of the POLG disease mutations in Europe, Australia, New Zealand, and the United States explained by single ancient European founders

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3101889

Phenotypic spectrum associated with mutations of the mitochondrial polymerase gamma gene

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3101889

Autosomal recessive mitochondrial ataxic syndrome due to mitochondrial polymerase gamma mutations

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3101889

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

26 October 2018

1 reference

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Mitochondrial dysfunction and psychiatric disorders

26 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21654874

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.2147/NDT.S20153

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21654874%20AND%20SRC:MED&resulttype=core&format=json

3 February 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21654874%20AND%20SRC:MED&resulttype=core&format=json

3 February 2020

PubMed publication ID

21654874

1 reference