(Q74069858)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9436802%20AND%20SRC:MED&resulttype=core&format=json

8 November 2019

title

Type IV 3-methylglutaconic (3-MGC) aciduria: a new case presenting with hepatic dysfunction (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9436802%20AND%20SRC:MED&resulttype=core&format=json

8 November 2019

author name string

E Broide

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9436802%20AND%20SRC:MED&resulttype=core&format=json

8 November 2019

O Elpeleg

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9436802%20AND%20SRC:MED&resulttype=core&format=json

8 November 2019

E Lahat

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9436802%20AND%20SRC:MED&resulttype=core&format=json

8 November 2019

publication date

1 November 1997

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9436802%20AND%20SRC:MED&resulttype=core&format=json

8 November 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9436802%20AND%20SRC:MED&resulttype=core&format=json

8 November 2019

volume

17

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9436802%20AND%20SRC:MED&resulttype=core&format=json

8 November 2019

issue

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9436802%20AND%20SRC:MED&resulttype=core&format=json

8 November 2019

page(s)

353-355

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9436802%20AND%20SRC:MED&resulttype=core&format=json

3-Methylglutaconyl-coenzyme-A hydratase deficiency: a new case

8 November 2019

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2897%2900096-9

7 January 2021

A novel X-linked gene, G4.5. is responsible for Barth syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2897%2900096-9

7 January 2021

X-linked dilated cardiomyopathy with neutropenia, growth retardation, and 3-methylglutaconic aciduria

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2897%2900096-9

7 January 2021

Behr syndrome: A clinicopathologic report

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2897%2900096-9

7 January 2021

A familial syndrome of infantile optic atrophy, movement disorder, and spastic paraplegia

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2897%2900096-9

7 January 2021

Phenotypic heterogeneity in the syndromes of 3-methylglutaconic aciduria

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2897%2900096-9

7 January 2021

Multiple syndromes of 3-methylglutaconic aciduria

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2897%2900096-9

7 January 2021

Fatal infantile mitochondrial cardiomyopathy and myopathy with heterogeneous tissue expression of combined respiratory chain deficiencies

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2897%2900096-9

7 January 2021

3-Methylglutaconic aciduria in a patient with a disturbed mitochondrial energy metabolism

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2897%2900096-9

7 January 2021

10.1016/S0887-8994(97)00096-9

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9436802%20AND%20SRC:MED&resulttype=core&format=json

8 November 2019

1 reference