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

Ursula Gresser (editor), R.A. De Abreu (contributions), J. Aimi (contributions), F.X. Arredondo-Vega (contributions), B.A. Barshop (contributions), M.T. Bausch-Jurken (contributions), F.Van den Bergh (contributions), G. Van den Berghe (contributions), P. Casaer (contributions), J. Chen (contributions), P. De Cock (contributions), B.L. Davidson (contributions), P.M. Davies (contributions), J.E. Dixon (contributions), J.A. Duley (contributions), W. Friedrich (contributions), B.S. Gathof (contributions), U. Gresser (contributions), M. Gross (contributions), W. Gutensohn (contributions), W. Hartmann (contributions), J.F. Hendersohn (contributions), M.J. Hendersohn (contributions), M.S. Hershfield (contributions), J. Jaeken (contributions), I. Kamilli (contributions), D.K. Mahnke-Zizelman (contributions), F.A. Mateos (contributions), B.S. Mitchell (contributions), J.G. Puig (contributions), B.J. Roessler (contributions), R.L. Sabina (contributions), A.S. Sahota (contributions), I. Santisteban (contributions), Y.S. Shin (con

Hardback (10 Aug 1993)

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Publisher's Synopsis

Explores the genetic basis, clinical aspects and biochemical foundations of hypoxanthine phosphoribosyltransferase deficiency, hyperuricaemia and gout, adenosine deaminase deficiency and adenine phosphoribosyltransferase deficiency.

Book information

ISBN:	9783540567745
Publisher:	Springer Berlin Heidelberg
Imprint:	Springer
Pub date:	10 Aug 1993
DEWEY:	611.01816
Language:	English
Number of pages:	182 .
Weight:	335g
Height:	216mm
Width:	138mm

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