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

9783642849640: Molecular Genetics, Biochemistry and Clinical Aspects of Inherited Disorders of Purine and Pyrimidine Metabolism
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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.

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  • PublisherSpringer
  • Publication date2011
  • ISBN 10 3642849644
  • ISBN 13 9783642849640
  • BindingPaperback
  • Number of pages196
  • EditorGresser Ursula

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9780387567747: Molecular Genetics, Biochemistry and Clinical Aspects of Inherited Disorders of Purine and Pyrimidine Metabolism

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ISBN 10:  0387567747 ISBN 13:  9780387567747
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  • 9783540567745: Molecular Genetics, Biochemistry and Clinical Aspects of Inherited Disorders of Purine and Pyrimidine Metabolism

    Springer, 1993
    Hardcover

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Book Description Taschenbuch. Condition: Neu. This item is printed on demand - it takes 3-4 days longer - 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. 200 pp. Englisch. Seller Inventory # 9783642849640

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Gresser, Ursula (Editor) / Abreu, R.A. De (Contributor) / Bergh, F.Van den (Contributor) / Davidson, B.L. (Contributor) / Dixon, J.E. (Contributor) / Davies, P.M. (Contributor) / Berghe, G. Van den (Contributor) / Duley, J.A. (Contributor)
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Gresser, Ursula|Abreu, R.A. De|Aimi, J.|Arredondo-Vega, F. X.|Barshop, B. A.|Bausch-Jurken, M. T.|Bergh, F.Van den|Berghe, G. Vanden|Casaer, P.|Chen, J.|Cock, P. De|Davidson, B. L.|Davies, P. M.|Dixon, J. E.|Duley, J. A.|Friedrich, W.|Gathof, B. S.|Gresse
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Book Description Condition: New. Dieser Artikel ist ein Print on Demand Artikel und wird nach Ihrer Bestellung fuer Sie gedruckt. I Purine Salvage Enzymes.- IA Hypoxanthine Guanine Phosphoribosyltransferase (HGPRT) Deficiency 3.- 1 Introductory Remarks.- 2 The Clinical Aspects of HGPRT Deficiency.- 3 The Biochemical Basis of HGPRT Deficiency.- 4 Prenatal Diagnosis of Lesch-Nyhan Syndr. Seller Inventory # 5072211

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Book Description Taschenbuch. Condition: Neu. Druck auf Anfrage Neuware - Printed after ordering - 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. Seller Inventory # 9783642849640

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. Ed(s): Gresser, Ursula
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Book Description Condition: New. 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. . 2011. Softcover reprint of the original 1st ed. 1993. Paperback. . . . . Seller Inventory # V9783642849640

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