(Q54175375)

English

Lesch-Nyhan syndrome: absence of the mutant enzyme in erythrocytes of a heterozygote for both normal and mutant hypoxanthine-guanine phosphoribosyl transferase.

scientific article published in February 1972

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

25 May 2018

http://europepmc.org/abstract/MED/4354247

Lesch-Nyhan syndrome: absence of the mutant enzyme in erythrocytes of a heterozygote for both normal and mutant hypoxanthine-guanine phosphoribosyl transferase. (English)

1 reference

Europe PubMed Central

PubMed publication ID

25 May 2018

http://europepmc.org/abstract/MED/4354247

Lesch-Nyhan syndrome

0 references

John A. McDonald

1

object named as

J A McDonald

0 references

author name string

W N Kelley

2

1 reference

Europe PubMed Central

PubMed publication ID

25 May 2018

http://europepmc.org/abstract/MED/4354247

publication date

1 February 1972

1 reference

Europe PubMed Central

PubMed publication ID

25 May 2018

http://europepmc.org/abstract/MED/4354247

Biochemical Genetics

1 reference

Europe PubMed Central

PubMed publication ID

25 May 2018

http://europepmc.org/abstract/MED/4354247

6

1 reference

Europe PubMed Central

PubMed publication ID

25 May 2018

http://europepmc.org/abstract/MED/4354247

1

1 reference

Europe PubMed Central

PubMed publication ID

25 May 2018

http://europepmc.org/abstract/MED/4354247

21-26

1 reference

Europe PubMed Central

PubMed publication ID

25 May 2018

http://europepmc.org/abstract/MED/4354247

https://scigraph.springernature.com/pub.10.1007/bf00485961

0 references

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/4354247

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Lesch-Nyhan syndrome: altered kinetic properties of mutant enzyme

1 reference

https://pubmed.ncbi.nlm.nih.gov/4354247

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Single-allele expression at an X-linked hyperuricemia locus in heterozygous human cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/4354247

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

X-linked hypoxanthine-guanine phosphoribosyl transferase deficiency: heterozygote has two clonal populations

1 reference

https://pubmed.ncbi.nlm.nih.gov/4354247

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A FAMILIAL DISORDER OF URIC ACID METABOLISM AND CENTRAL NERVOUS SYSTEM FUNCTION

1 reference

https://pubmed.ncbi.nlm.nih.gov/4354247

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Dependence of Bone Marrow Cells on the Liver for Purine Supply

1 reference

https://pubmed.ncbi.nlm.nih.gov/4354247

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

X-linked hypoxanthine-guanine phosphoribosyl transferase deficiency: Detection of heterozygotes by selective medium

1 reference

https://pubmed.ncbi.nlm.nih.gov/4354247

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Effects of allopurinol and oxipurinol on purine synthesis in cultured human cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/4354247

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Gene action in the X-chromosome of the mouse (Mus musculus L.)

1 reference

https://pubmed.ncbi.nlm.nih.gov/4354247

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hypoxanthine-Guanine Phosphoribosyltransferase Deficiency in Gout

1 reference

https://pubmed.ncbi.nlm.nih.gov/4354247

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/4354247

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hemizygous expression of glucose-6-phosphate dehydrogenase in erythrocytes of heterozygotes for the Lesch-Nyhan syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/4354247

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hypoxanthine-guanine phosphoribosyltransferase deficiency in the Lesch-Nyhan syndrome and gout

1 reference

https://pubmed.ncbi.nlm.nih.gov/4354247

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00485961

1 reference

Europe PubMed Central

PubMed publication ID

25 May 2018

http://europepmc.org/abstract/MED/4354247

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

25 May 2018

http://europepmc.org/abstract/MED/4354247

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q54175375&oldid=1384415359"