Using Next-Generation Sequencing to Identify a Mutation in Human MCSU that is Responsible for Type II Xanthinuria

Background: Hypouricemia is caused by various diseases and disorders, such as hepatic failure, Fanconi renotubular syndrome, nutritional deficiencies and genetic defects. Genetic defects of the molybdoflavoprotein enzymes induce hypouricemia and xanthinuria. Here, we identified a patient whose plasm...

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Bibliografiset tiedot

Päätekijät:	Yunan Zhou, Xueguang Zhang, Rui Ding, Zuoxiang Li, Quan Hong, Yan Wang, Wei Zheng, Xiaodong Geng, Meng Fan, Guangyan Cai, Xiangmei Chen, Di Wu
Aineistotyyppi:	Artigo
Kieli:	Inglês
Julkaistu:	Cell Physiol Biochem Press GmbH & Co KG 2015-04-01
Sarja:	Cellular Physiology and Biochemistry
Aiheet:	Hypouricemia Xanthinuria Human molybdenum cofactor sulfurase (MCSU) Xanthine dehydrogenase (XDH) and Xanthine oxidase (XOD)
Linkit:	http://www.karger.com/Article/FullText/374042
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