Molecular Genetics, Biochemistry and Clinical Aspects of Inherited Disorders of Purine and Pyrimidine Metabolism

Gresser, Ursula (Editor) / Abreu, R.A. De (Contributor) / Bergh, F.Van den (Contributor) / Davidson, B.L. (Contributor) / Dixon, J.E. (Contributor) / Davies, P.M. (Contributor) / Berghe, G. Van den (Contributor) / Duley, J.A. (Contributor)

ISBN 10: 3642849644 / ISBN 13: 9783642849640

Published by Springer-Verlag, 2011

About this Item

reprint edition. 196 pages. 7.90x5.20x0.50 inches. In Stock.

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Bibliographic Details

• Title: Molecular Genetics, Biochemistry and Clinical Aspects of Inherited Disorders of Purine and Pyrimidine Metabolism
• Publisher: Springer-Verlag
• Publication Date: 2011
• Language: English
• ISBN 10: 3642849644
• ISBN 13: 9783642849640
• Binding: Paperback
• Condition: Brand New
• Weight: 0.23 kilograms

About this title

Synopsis

Inherited disorders of purine and pyrimidine metabolism in man lead to severe diseases. At the 2nd M}nchner Adventssymposium the state of the art as to the genetic basis, clinical aspects, and the biochemical basis has been given by leading experts in the fields concerning the following diseases: Hypoxanthine phosphoribosyltransferase deficiency (HGPRT-deficieny), adenine phosphoribosyltransferase deficiency (APRT-deficiency), hyperuricemia and gout, adenosine deaminase deficiency (ADA-deficiency, purine nucleoside phosphorylase deficiency (PNP-deficiency). All contributions of the symposium are published within this volume thus giving and overview of this most interesting field.