Amino acid and enzyme studies of brain and other tissues in an infant with argininosuccinic aciduria-Reference-Cited by-同舟云学术

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Amino acid and enzyme studies of brain and other tissues in an infant with argininosuccinic aciduria

Published:1980-08 Issue:2 Volume:105 Page:257-267
ISSN:0009-8981
Container-title:Clinica Chimica Acta
language:en
Short-container-title:Clinica Chimica Acta

Author:

Perry Thomas L.,Wirtz Mary L.K.,Kennaway Nancy G.,Edward Hsia Y.,Atienza Fernando C.,Uemura Herbert S.

Publisher

Elsevier BV

Subject

Biochemistry (medical),Clinical Biochemistry,Biochemistry,General Medicine

Reference26 articles.

1. Inherited Hyperammonemic Syndromes

2. The Metabolic Basis of Inherited Disease;Shih,1978

3. REGIONAL DISTRIBUTION OF AMINO ACIDS IN HUMAN BRAIN OBTAINED AT AUTOPSY

Cited by 22 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Identification of mutations in Malaysian patients with argininosuccinate lyase (ASL) deficiency;Molecular Genetics and Metabolism Reports;2019-12

2. Amino Acids;Volpe's Neurology of the Newborn;2018

3. Understanding the Role of Argininosuccinate Lyase Transcript Variants in the Clinical and Biochemical Variability of the Urea Cycle Disorder Argininosuccinic Aciduria;Journal of Biological Chemistry;2013-11

4. Bacterial expression of mutant argininosuccinate lyase reveals imperfect correlation of in-vitro enzyme activity with clinical phenotype in argininosuccinic aciduria;Journal of Inherited Metabolic Disease;2011-06-11

5. Neurotransmitter glutamate: its clinical importance;Acta Neurologica Scandinavica;2009-01-29

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