(Q51583597)

7 April 2018

title

Mitochondrial short-chain L-3-hydroxyacyl-coenzyme A dehydrogenase deficiency: a new defect of fatty acid oxidation. (English)

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7 April 2018

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Bennett MJ

1

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7 April 2018

Weinberger MJ

2

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7 April 2018

Kobori JA

3

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Rinaldo P

4

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7 April 2018

Burlina AB

5

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7 April 2018

language of work or name

English

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publication date

1 January 1996

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7 April 2018

published in

Pediatric Research

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volume

39

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7 April 2018

issue

1

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7 April 2018

page(s)

185-188

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7 April 2018

https://scigraph.springernature.com/pub.10.1203/00006450-199601000-00031

exact match

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cites work

Fatty acid oxidation disorders: A new class of metabolic diseases

1 reference

https://api.crossref.org/works/10.1203%2F00006450-199601000-00031

The enzymes of mitochondrial fatty acid oxidation

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F00006450-199601000-00031

Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: identification of a new inborn error of mitochondrial fatty acid beta-oxidation

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F00006450-199601000-00031

Hypoglycemia in infancy and childhood. II.

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F00006450-199601000-00031

Short-chainL-3-hydroxyacyl-CoA dehydrogenase deficiency in muscle: A new cause for recurrent myoglobinuria and encephalopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F00006450-199601000-00031

10.1203/00006450-199601000-00031

21 January 2018

Identifiers

DOI

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7 April 2018

Dimensions Publication ID

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7 April 2018