Molecular Genetics, Biochemistry and Clinical Aspects of Inherited Disorders of Purine and Pyrimidine Metabolism
R. W. E. Watts (auth.), Privat-Dozentin Dr. Ursula Gresser (eds.)
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.
Categorie:
Anno:
1993
Edizione:
1
Casa editrice:
Springer-Verlag Berlin Heidelberg
Lingua:
english
Pagine:
182
ISBN 10:
3642849644
ISBN 13:
9783642849640
File:
PDF, 9.19 MB
IPFS:
,
english, 1993
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