Molecular Genetics, Biochemistry and Clinical Aspects of Inherited Disorders of Purine and Pyrimidine Metabolism
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.
1103063223
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.
Molecular Genetics, Biochemistry and Clinical Aspects of Inherited Disorders of Purine and Pyrimidine Metabolism
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.
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.
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Molecular Genetics, Biochemistry and Clinical Aspects of Inherited Disorders of Purine and Pyrimidine Metabolism
182Molecular Genetics, Biochemistry and Clinical Aspects of Inherited Disorders of Purine and Pyrimidine Metabolism
182Paperback(Softcover reprint of the original 1st ed. 1993)
$109.99
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Product Details
ISBN-13: | 9783642849640 |
---|---|
Publisher: | Springer Berlin Heidelberg |
Publication date: | 12/15/2011 |
Edition description: | Softcover reprint of the original 1st ed. 1993 |
Pages: | 182 |
Product dimensions: | 5.24(w) x 7.99(h) x 0.02(d) |
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