(Q28284029)

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Adenine phosphoribosyltransferase: a simple spectrophotometric assay and the incidence of mutation in the normal population

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Adenine phosphoribosyltransferase: a simple spectrophotometric assay and the incidence of mutation in the normal population (English)

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ORCID Public Data File 2021

author name string

L A Johnson

series ordinal

1

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R B Gordon

series ordinal

2

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B T Emmerson

series ordinal

3

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language of work or name

English

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publication date

April 1977

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published in

Biochemical Genetics

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volume

15

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page(s)

265-72

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issue

3-4

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cites work

A specific enzyme defect in gout associated with overproduction of uric acid

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/869896

retrieved

12 December 2020

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inferred from PubMed ID database lookup

Adenine phosphoribosyltransferase deficiency in man. Report of a second family

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/869896

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A spectrophotometric assay for hypoxanthine-guanine phosphoribosyltransferase

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stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/869896

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[A new metabolic disease: the complete deficit of adenine phosphoribosyltransferase and lithiasis of 2,8-dihydroxyadenine]

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stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/869896

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Adenine phosphoribosyltransferase deficiency: its inheritance and occurrence in a female with gout and renal disease

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stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/869896

retrieved

12 December 2020

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Protein measurement with the Folin phenol reagent

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stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/869896

retrieved

12 December 2020

based on heuristic

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Purine metabolism in heterozygous carriers of hypoxanthine-guanine phosphoribosyltransferase deficiency

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stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/869896

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Adenine phosphoribosyltransferase deficiency: a previously undescribed genetic defect in man

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/869896

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Enzyme Defect Associated with a Sex-Linked Human Neurological Disorder and Excessive Purine Synthesis

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stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/869896

retrieved

12 December 2020

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Identifiers

DOI

10.1007/BF00484458

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1049955123

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release_f6ghw2z555fsjm2iwyznbkzdfy

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https://api.fatcat.wiki/v0/release/f6ghw2z555fsjm2iwyznbkzdfy

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24 November 2022

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PubMed ID

869896

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ResearchGate publication ID

22284837

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Springer Nature article ID

10.1007/bf00484458

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(Q28284029)

Adenine phosphoribosyltransferase: a simple spectrophotometric assay and the incidence of mutation in the normal population

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