(Q68363942)

English

A bifunctional protein with deficient enzymic activity: identification of a new peroxisomal disorder using novel methods to measure the peroxisomal beta-oxidation enzyme activities

scientific article published on 01 January 1990

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scholarly article

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2122104%20AND%20SRC:MED&resulttype=core&format=json

23 September 2019

A bifunctional protein with deficient enzymic activity: identification of a new peroxisomal disorder using novel methods to measure the peroxisomal beta-oxidation enzyme activities (English)

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2122104%20AND%20SRC:MED&resulttype=core&format=json

23 September 2019

author name string

R J Wanders

1

1 reference

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23 September 2019

C W van Roermund

2

1 reference

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23 September 2019

A Schelen

3

1 reference

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23 September 2019

R B Schutgens

4

1 reference

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23 September 2019

J M Tager

5

1 reference

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23 September 2019

J B Stephenson

6

1 reference

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23 September 2019

P T Clayton

7

1 reference

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23 September 2019

publication date

1 January 1990

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23 September 2019

Journal of Inherited Metabolic Disease

1 reference

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23 September 2019

13

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23 September 2019

375-379

1 reference

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23 September 2019

3

1 reference

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23 September 2019

https://scigraph.springernature.com/pub.10.1007/bf01799399

0 references

The inborn errors of peroxisomal beta-oxidation: a review

1 reference

https://pubmed.ncbi.nlm.nih.gov/2122104

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Peroxisomal bifunctional enzyme deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/2122104

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Bile acid analyses in "pseudo-Zellweger" syndrome; clues to the defect in peroxisomal beta-oxidation

1 reference

https://pubmed.ncbi.nlm.nih.gov/2122104

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Neonatal seizures and retardation in a girl with biochemical features of X-linked adrenoleukodystrophy: a possible new peroxisomal disease entity

1 reference

https://pubmed.ncbi.nlm.nih.gov/2122104

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF01799399

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2122104%20AND%20SRC:MED&resulttype=core&format=json

23 September 2019

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2122104%20AND%20SRC:MED&resulttype=core&format=json

23 September 2019

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