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A familial study of a human enzyme defect, argininosuccinic aciduria

  • Published:1964-01 Issue:4 Volume:14 Page:307-312
  • ISSN:0006-291X
  • Container-title:Biochemical and Biophysical Research Communications
  • language:en
  • Short-container-title:Biochemical and Biophysical Research Communications

Author:

Coryell Margaret E.,Knowlton Hall W.,Thevaos Theo G.,Welter Dave A.,Gatz Arthur J.,Horton Bennett F.,Sisson Boyd D.,Looper John W.,Farrow Royal T.

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Biochemistry,Biophysics

Cited by 32 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. Argininosuccinate lyase deficiency;Genetics in Medicine;2012-05

2. Argininosuccinate lyase deficiency-Argininosuccinic aciduria and beyond;American Journal of Medical Genetics Part C: Seminars in Medical Genetics;2011-02-10

3. Disorders of the Metabolism of Amino Acids and Related Compounds;Genetic Disorders and the Fetus;2010-09-24

4. ARGININOSUCCINIC ACIDURIA: CLINICAL, BIOCHEMICAL, ANATOMICAL AND NEUROPATHOLOGICAL OBSERVATIONS*;Journal of Intellectual Disability Research;2008-06-28

5. Antenatal diagnosis of argininosuccinic aciduria;Clinical Genetics;2008-04-23
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