Hereditary disorders of purine and pyrimidine metabolism: identification of their biochemical phenotypes in the clinical laboratory.-Reference-Cited by-同舟云学术

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Hereditary disorders of purine and pyrimidine metabolism: identification of their biochemical phenotypes in the clinical laboratory.

Published:1997-08-01 Issue:8 Volume:72 Page:719-725
ISSN:0025-6196
Container-title:Mayo Clinic Proceedings
language:en
Short-container-title:Mayo Clinic Proceedings

Author:

Valik D,Jones J D

Publisher

Elsevier BV

Subject

General Medicine

Cited by 3 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. Detection of urinary metabolites of metabolic pathway disorders by using VTGE and LC-HRMS techniques;2019-10-23

2. Uracil salvage pathway in PC12 cells;Biochimica et Biophysica Acta (BBA) - General Subjects;2000-11-15

3. Ribose 1-phosphate and inosine activate uracil salvage in rat brain;Biochimica et Biophysica Acta (BBA) - General Subjects;1999-10

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