Report on a new patient with combined deficiencies of sulphite oxidase and xanthine dehydrogenase due to molybdenum cofactor deficiency
Author:
Publisher
Springer Science and Business Media LLC
Subject
Pediatrics, Perinatology and Child Health
Link
http://link.springer.com/content/pdf/10.1007/BF00441412.pdf
Reference18 articles.
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2. Barth PG, Beemer FA, Cats BP, Duran M, Wadman SK (1985) Neurological findings in a case of combined deficiency of sulphite oxidase and xanthine dehydrogenase. Virchow's Arch [A] 408: 105?106
3. Duran M, Beemer FA, Heiden C van der, Korteland J, Bree PK de, Brink M, Wadman SK (1978) Combined deficiency of xanthine oxidase and sulphite oxidase: a defect of molybdenum metabolism or transport? J Inherited Metab Dis 1:175?178
4. Endres W, Seibold H (1978) Renal excretion of cystathionine and creatinine in humans at different ages. Clin Chim Acta 87:425?432
5. Frayha RA, Salti IS, Araout RA, Katchadurian A, Uhtman SM (1977) Hereditary xanthinuria, report on three patients and short review of the literature. Nephron 19:328?332
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