(Q48216411)

English

An intronic duplication in the alanine: glyoxylate aminotransferase gene facilitates identification of mutations in compound heterozygote patients with primary hyperoxaluria type 1.

scientific article published in August 1991

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scholarly article

1 reference

Europe PubMed Central

9 February 2018

http://europepmc.org/abstract/MED/1879825

An intronic duplication in the alanine: glyoxylate aminotransferase gene facilitates identification of mutations in compound heterozygote patients with primary hyperoxaluria type 1. (English)

1 reference

Europe PubMed Central

9 February 2018

http://europepmc.org/abstract/MED/1879825

1 reference

based on heuristic

inferred from title

primary hyperoxaluria

1 reference

based on heuristic

inferred from title

author name string

P E Purdue

1

1 reference

Europe PubMed Central

9 February 2018

http://europepmc.org/abstract/MED/1879825

M J Lumb

2

1 reference

Europe PubMed Central

9 February 2018

http://europepmc.org/abstract/MED/1879825

J Allsop

3

1 reference

Europe PubMed Central

9 February 2018

http://europepmc.org/abstract/MED/1879825

C J Danpure

4

1 reference

Europe PubMed Central

9 February 2018

http://europepmc.org/abstract/MED/1879825

publication date

1 August 1991

1 reference

Europe PubMed Central

9 February 2018

http://europepmc.org/abstract/MED/1879825

1 reference

Europe PubMed Central

9 February 2018

http://europepmc.org/abstract/MED/1879825

87

1 reference

Europe PubMed Central

9 February 2018

http://europepmc.org/abstract/MED/1879825

4

1 reference

Europe PubMed Central

9 February 2018

http://europepmc.org/abstract/MED/1879825

394-396

1 reference

Europe PubMed Central

9 February 2018

http://europepmc.org/abstract/MED/1879825

https://scigraph.springernature.com/pub.10.1007/bf00197154

0 references

Human peroxisomal L-alanine: glyoxylate aminotransferase. Evolutionary loss of a mitochondrial targeting signal by point mutation of the initiation codon

1 reference

https://pubmed.ncbi.nlm.nih.gov/1879825

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Characterization and chromosomal mapping of a genomic clone encoding human alanine:glyoxylate aminotransferase

1 reference

https://pubmed.ncbi.nlm.nih.gov/1879825

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Peroxisomal alanine:glyoxylate aminotransferase deficiency in primary hyperoxaluria type I

1 reference

https://pubmed.ncbi.nlm.nih.gov/1879825

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of mutations associated with peroxisome-to-mitochondrion mistargeting of alanine/glyoxylate aminotransferase in primary hyperoxaluria type 1

1 reference

https://pubmed.ncbi.nlm.nih.gov/1879825

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Domain characterization of rabbit skeletal muscle myosin light chain kinase.

1 reference

https://pubmed.ncbi.nlm.nih.gov/1879825

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00197154

1 reference

Europe PubMed Central

9 February 2018

http://europepmc.org/abstract/MED/1879825

1 reference

Europe PubMed Central

9 February 2018

http://europepmc.org/abstract/MED/1879825

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