(Q48183315)

9 February 2018

title

Bilateral striatal necrosis associated with a novel mutation in the mitochondrial ND6 gene (English)

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16 March 2024

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16 March 2024

author name string

Abelardo Solano

1

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9 February 2018

Manuel Roig

2

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9 February 2018

Cristofol Vives-Bauza

3

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9 February 2018

Jose Hernandez-Peña

4

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9 February 2018

Elena Garcia-Arumi

5

1 reference

9 February 2018

Ana Playan

6

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9 February 2018

Julio Montoya

9

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9 February 2018

Manuel J. Lopez-Perez

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A14520668

16 March 2024

Antonio L. Andreu

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A14520668

16 March 2024

language of work or name

English

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=14520668

16 March 2024

publication date

1 October 2003

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9 February 2018

full work available at URL

number of pages

4

1 reference

based on heuristic

inferred from page(s)

https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fana.10682

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https://onlinelibrary.wiley.com/doi/pdf/10.1002/ana.10682

16 March 2024

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16 March 2024

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9 February 2018

volume

54

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9 February 2018

issue

4

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9 February 2018

page(s)

527-530

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9 February 2018

Lessons from mitochondrial DNA mutations

cites work

1 reference

Automating the identification of DNA variations using quality-based fluorescence re-sequencing: analysis of the human mitochondrial genome

21 January 2018

1 reference

Human cells lacking mtDNA: repopulation with exogenous mitochondria by complementation

21 January 2018

1 reference

Mitochondrial DNA nucleotide changes C14482G and C14482A in the ND6 gene are pathogenic for Leber's hereditary optic neuropathy.

21 January 2018

1 reference

Electron transfer complex I defect in idiopathic dystonia

21 January 2018

1 reference

Leigh-like encephalopathy complicating Leber's hereditary optic neuropathy

21 January 2018

1 reference

Bilateral striatal necrosis with a novel point mutation in the mitochondrial ATPase 6 gene

21 January 2018

1 reference

Leigh disease caused by the mitochondrial DNA G14459A mutation in unrelated families

21 January 2018

1 reference

Exercise intolerance due to a nonsense mutation in the mtDNA ND4 gene

21 January 2018

1 reference

Detection of MELAS A3243G point mutation in muscle, blood and hair follicles

21 January 2018

1 reference

Biochemical features of mtDNA 14484 (ND6/M64V) point mutation associated with Leber's hereditary optic neuropathy

21 January 2018

1 reference

Mitochondrial DNA in focal dystonia: A cybrid analysis

21 January 2018

1 reference

A novel mitochondrial ATPase 6 point mutation in familial bilateral striatal necrosis

21 January 2018

1 reference

21 January 2018

Identifiers

DOI

10.1002/ANA.10682

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9 February 2018

release_ugr6eha4hrcelkwzceihc2dvry

Fatcat ID

0 references

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9 February 2018