Identification of mutations in Malaysian patients with argininosuccinate lyase (ASL) deficiency-Reference-Cited by-同舟云学术

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Identification of mutations in Malaysian patients with argininosuccinate lyase (ASL) deficiency

Published:2019-12 Issue: Volume:21 Page:100525
ISSN:2214-4269
Container-title:Molecular Genetics and Metabolism Reports
language:en
Short-container-title:Molecular Genetics and Metabolism Reports

Author:

Ali Ernie Zuraida,Yakob Yusnita,Ngu Lock Hock

Funder

Diagnostics Services, Institute for Medical Research, Ministry of Health, Malaysia

Publisher

Elsevier BV

Subject

Endocrinology,Genetics,Molecular Biology

Reference39 articles.

1. Argininosuccinate lyase: purification and characterization from human liver;O’Brien;Biochemistry,1981

2. Cloning and sequence analysis of cDNA for human argininosuccinate Iyase (urea cycle/genetic disorders/chrpmosome mapping);O’Brien;Proc. Natl. Acad. Sci. U. S. A.,1986

3. The incidence of urea cycle disorders;Summar;Mol. Genet. Metab.,2013

4. Suggested guidelines for the diagnosis and management of urea cycle disorders;Häberle;Orphanet. J. Rare Dis.,2012

5. Argininosuccinic aciduria: assignment of the argininosuccinate lyase gene to the pter-q22 region of human chromosome 7 by bioautography (somatic cell hybrids/aminoaciduria);Naylor;Proc. Natl. Acad. Sci. U. S. A.,1978

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1. Prediction of driver variants in the cancer genome via machine learning methodologies;Briefings in Bioinformatics;2020-10-22

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