Molecular Genetics, Biochemistry and Clinical Aspects of Inherited Disorders of Purine and Pyrimidine Metabolism
Language: English
Published by Springer Berlin Heidelberg, Springer Vieweg Dez 2011, 2011
- Softcover
- New
Seller: buchversandmimpf2000, Emtmannsberg, BAYE, Germanybuchversandmimpf2000
AbeBooks seller since January 23, 2017
Condition: New
£ 94.74
Quantity: 1 available
Add to basketItem description from seller
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
- Title
- Molecular Genetics, Biochemistry and Clinical Aspects of Inherited Disorders of Purine and Pyrimidine Metabolism
- Author
- Ursula Gresser
- Publisher
- Springer Berlin Heidelberg, Springer Vieweg Dez 2011
- Publication year
- 2011
- Condition
- Neu
- Binding
- Taschenbuch
- Language
- English
- ISBN 10
- 3642849644
- ISBN 13
- 9783642849640
- Item weight
- 231 grams
- Dimensions
- 203x133x12 mm
"Synopsis" may belong to another edition of this title.
buchversandmimpf2000
Emtmannsberg, BAYE, Germany
AbeBooks seller since January 23, 2017
Shipping rates from Germany to U.S.A.
| Item | 60 to 60 business days | 60 to 60 business days |
|---|---|---|
| First item | £ 51.59 | £ 64.48 |
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