(Q46715707)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16178026%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

title

Late-onset MNGIE due to partial loss of thymidine phosphorylase activity (English)

1 reference

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7 January 2020

1

1 reference

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7 January 2020

Jan J Verschuuren

2

1 reference

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7 January 2020

author name string

Alan Buchman

3

1 reference

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7 January 2020

Ikuo Hirano

4

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7 January 2020

Saba Tadesse

5

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7 January 2020

André B P van Kuilenburg

6

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7 January 2020

Albert H van Gennip

7

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7 January 2020

Ben J H M Poorthuis

8

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7 January 2020

Michio Hirano

9

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7 January 2020

publication date

1 October 2005

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7 January 2020

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7 January 2020

volume

58

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7 January 2020

issue

4

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7 January 2020

page(s)

649-652

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Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE): clinical, biochemical, and genetic features of an autosomal recessive mitochondrial disorder

7 January 2020

cites work

1 reference

Partial depletion and multiple deletions of muscle mtDNA in familial MNGIE syndrome.

21 January 2018

1 reference

Organization and chromosomal localization of the human platelet-derived endothelial cell growth factor gene

21 January 2018

1 reference

Lack of gastrointestinal symptoms in a 60-year-old patient with MNGIE.

21 January 2018

1 reference

21 January 2018

Identifiers

DOI

10.1002/ANA.20615

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16178026%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

1 reference