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

Ursula Gresser

ISBN 10: 3642849644 / ISBN 13: 9783642849640

Published by Springer Berlin Heidelberg, Springer Vieweg Dez 2011, 2011

About this Item

This item is printed on demand - Print on Demand Titel. Neuware -Inherited disorders of purine and pyrimidine metabolism inman lead to severe diseases. At the 2nd M}nchnerAdventssymposium the state of the art as to the geneticbasis, clinical aspects, and the biochemical basis has beengiven by leading experts in the fields concerning thefollowing diseases: Hypoxanthine phosphoribosyltransferasedeficiency (HGPRT-deficieny), adeninephosphoribosyltransferase deficiency (APRT-deficiency)hyperuricemia and gout, adenosine deaminase deficiency(ADA-deficiency, purine nucleoside phosphorylase deficiency(PNP-deficiency). All contributions of the symposium arepublished within this volume thus giving and overview ofthis most interesting field.Springer-Verlag GmbH, Tiergartenstr. 17, 69121 Heidelberg 200 pp. Englisch.

Seller Inventory # 9783642849640

Bibliographic Details

• Title: Molecular Genetics, Biochemistry and Clinical Aspects of Inherited Disorders of Purine and Pyrimidine Metabolism
• Publisher: Springer Berlin Heidelberg, Springer Vieweg Dez 2011
• Publication Date: 2011
• Language: English
• ISBN 10: 3642849644
• ISBN 13: 9783642849640
• Binding: Taschenbuch
• Condition: Neu
• Dimensions: 203W x 133H x 12D millimeters 203 millimeters width by 133 millimeters height by 12 millimeters depth
• Weight: 231 grams

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.