(Q68489826)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4259536%20AND%20SRC:MED&resulttype=core&format=json

24 September 2019

title

A distinct biochemical deficit in the Maroteaux-Lamy syndrome (mucopolysaccharidosis VI) (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4259536%20AND%20SRC:MED&resulttype=core&format=json

24 September 2019

main subject

mucopolysaccharidosis VI

1 reference

R W Baron

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4259536%20AND%20SRC:MED&resulttype=core&format=json

24 September 2019

E F Neufeld

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4259536%20AND%20SRC:MED&resulttype=core&format=json

24 September 2019

language of work or name

English

0 references

publication date

1 January 1972

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4259536%20AND%20SRC:MED&resulttype=core&format=json

The Journal of Pediatrics

24 September 2019

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4259536%20AND%20SRC:MED&resulttype=core&format=json

24 September 2019

volume

80

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4259536%20AND%20SRC:MED&resulttype=core&format=json

24 September 2019

issue

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4259536%20AND%20SRC:MED&resulttype=core&format=json

24 September 2019

page(s)

114-116

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4259536%20AND%20SRC:MED&resulttype=core&format=json

Inborn errors of mucopolysaccharide metabolism

24 September 2019

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2872%2980467-0

The defect in Hurler and Hunter syndromes. II. Deficiency of specific factors involved in mucopolysaccharide degradation

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2872%2980467-0

Characterization of the factor deficient in the Hunter syndrome by polyacrylamide gel electrophoresis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2872%2980467-0

Scheie and Hurler syndromes: apparent identity of the biochemical defect

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2872%2980467-0

Biochemical heterogeneity of the Sanfilippo syndrome: preliminary characterization of two deficient factors

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2872%2980467-0

Corrective factors for inborn errors of mucopolysaccharide metabolism

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2872%2980467-0

Induced degradation of glycosaminoglycans in Hurler's and Hunter's syndromes by plasma infusion

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2872%2980467-0

10.1016/S0022-3476(72)80467-0

7 January 2021

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4259536%20AND%20SRC:MED&resulttype=core&format=json

24 September 2019

1 reference