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Publications by Noriaki Iino
A Case of Xanthinuria Type I With a Novel Mutation in Xanthine Dehydrogenase
CEN Case Reports
Nephrology
Related publications
Identification of Two Mutations in Human Xanthine Dehydrogenase Gene Responsible for Classical Type I Xanthinuria.
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A Case of Vitamin D-Dependent Rickets Type 1A With a Novel Mutation in the Uzbek Population
JCRPE Journal of Clinical Research in Pediatric Endocrinology
Child Health
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Asymptomatic Hereditary Xanthinuria: A Case Report.
Japanese Journal of Medicine
A Novel TRPS1 Mutation in a Moroccan Family With Tricho-Rhino-Phalangeal Syndrome Type III: Case Report
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A Novel Mutation of KRT14 Gene in a Newborn With Epidermolysis Bullosa Simplex (Dowling-Meara Type): Case Report
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Xanthine Dehydrogenase/Xanthine Oxidase and Oxidative Stress
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Identification of a Novel Nonsense Mutation in SH2D1A in a Patient With X-Linked Lymphoproliferative Syndrome Type 1: A Case Report
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The Molybdenum Centers of Xanthine Oxidase and Xanthine Dehydrogenase
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Biochemistry
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The Conversion From the Dehydrogenase Type to the Oxidase Type of Rat Liver Xanthine Dehydrogenase by Modification of Cysteine Residues With Fluorodinitrobenzene
Journal of Biological Chemistry
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