(Q39377878)

11 September 2017

title

Letter: Aspartylglycosaminuria in Northern Norway (English)

1 reference

11 September 2017

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O Borud

1

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11 September 2017

K H Torp

series ordinal

2

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11 September 2017

language of work or name

English

0 references

publication date

1 May 1976

1 reference

11 September 2017

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11 September 2017

volume

1

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11 September 2017

issue

7968

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11 September 2017

page(s)

1082-1083

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Aspartylglycosaminuria. An inborn error of metabolism associated with mental defect.

11 September 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2876%2992266-2

7 January 2021

Detection of heterozygotes for aspartylglucosaminuria (AGU) in cultured fibroblasts

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2876%2992266-2

7 January 2021

Aspartylglucosaminuria: psychomotor retardation masquerading as a mucopolysaccharidosis

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2876%2992266-2

7 January 2021

Glycoasparagine metabolites in patients with aspartylglycosaminuria: comparison between english and finnish patients with special reference to storage materials

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2876%2992266-2

7 January 2021

Radioimmunoassay of proteins with the use of Sephadex-coupled antibodies

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2876%2992266-2

7 January 2021

Quantitative estimation of proteins by electrophoresis in agarose gel containing antibodies

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2876%2992266-2

7 January 2021

10.1016/S0140-6736(76)92266-2

Identifiers

DOI

1 reference

release_gi3765ff55hdvmjga4sfrhxa2e

11 September 2017

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/gi3765ff55hdvmjga4sfrhxa2e

24 November 2022

mapped directly with Wikidata item

1 reference