Mutation in the Human HPRT1 Gene and the Lesch-Nyhan Syndrome-Reference-Cited by-同舟云学术

Mutation in the Human HPRT1 Gene and the Lesch-Nyhan Syndrome

Published:2016-07-05 Issue:8 Volume:35 Page:426-434
ISSN:1525-7770
Container-title:Nucleosides, Nucleotides & Nucleic Acids
language:en
Short-container-title:Nucleosides, Nucleotides & Nucleic Acids

Author:

Nguyen Khue Vu¹²,Nyhan William L.²

Affiliation:

1. Department of Medicine, Biochemical Genetics and Metabolism, The Mitochondrial and Metabolic Disease Center, School of Medicine, University of California, San Diego, California, USA

2. Department of Pediatrics, University of California, San Diego, School of Medicine, San Diego, California, USA

Publisher

Informa UK Limited

Subject

Genetics,Molecular Medicine,Biochemistry,General Medicine

Link

https://www.tandfonline.com/doi/pdf/10.1080/15257770.2015.1098660

Reference19 articles.

1. A familial disorder of uric acid metabolism and central nervous system function

2. Enzyme Defect Associated with a Sex-Linked Human Neurological Disorder and Excessive Purine Synthesis

3. Fine structure of the human hypoxanthine phosphoribosyltransferase gene.

4. Novel Mutations in the Human HPRT Gene

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