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Ursula . Ed(S): Gresser - Molecular Genetics, Biochemistry and Clinical Aspects of Inherited Disorders of Purine and Pyrimidine Metabolism - 9783642849640 - V9783642849640
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Molecular Genetics, Biochemistry and Clinical Aspects of Inherited Disorders of Purine and Pyrimidine Metabolism

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Description for Molecular Genetics, Biochemistry and Clinical Aspects of Inherited Disorders of Purine and Pyrimidine Metabolism Paperback. Editor(s): Gresser, Ursula. Num Pages: 182 pages, 41 black & white tables, biography. BIC Classification: MBGR; MFGM. Category: (P) Professional & Vocational. Dimension: 203 x 133 x 11. Weight in Grams: 234.
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.

Product Details

Format
Paperback
Publication date
2011
Publisher
Springer-Verlag Berlin and Heidelberg GmbH & Co. KG Germany
Number of pages
182
Condition
New
Number of Pages
182
Place of Publication
Berlin, Germany
ISBN
9783642849640
SKU
V9783642849640
Shipping Time
Usually ships in 15 to 20 working days
Ref
99-15

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