Hereditary xanthinuria is not so rare disorder of purine metabolism-Reference-Cited by-同舟云学术

Hereditary xanthinuria is not so rare disorder of purine metabolism

Published:2018-05-03 Issue:6 Volume:37 Page:324-328
ISSN:1525-7770
Container-title:Nucleosides, Nucleotides and Nucleic Acids
language:en
Short-container-title:Nucleosides, Nucleotides and Nucleic Acids

Author:

Sebesta I.¹²,Stiburkova B.¹³^ORCID,Krijt J.¹

Affiliation:

1. Institute of Inherited Metabolic Disorders, First Faculty of Medicine, Charles University, Prague, Czech Republic

2. Institute of Medical Biochemistry and Laboratory Diagnostics, First Faculty of Medicine, Charles University, Prague, Czech Republic

3. Institute of Rheumatology, First Faculty of Medicine, Charles University, Prague, Czech Republic

Funder

Grantová Agentura, Univerzita Karlova

Publisher

Informa UK Limited

Subject

Genetics,Molecular Medicine,Biochemistry,General Medicine

Link

https://www.tandfonline.com/doi/pdf/10.1080/15257770.2018.1460478

Reference13 articles.

1. Xanthinuria, psoriasis and arthritis

2. Marcet, A. An Essay on the Chemical History and Medical Treatment of Calculous Disorders, 2nd ed. Longman: Hurst, Rees, Orme, and Brown London, London, 1819.

3. Simmonds, H. A. Hereditary & medically – induced xanthine oxidase deficiency (XOD); J. S. Cameron; H. A. Simmonds, Eds. PUMPA: Tansleys, Seaford, East Sussex, 2007; pp. 4.

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