Molecular Genetics, Biochemistry and Clinical Aspects of Inherited Disorders of Purine and Pyrimidine Metabolism
-
- Englisch ausgewählt
Fr. 137.00
inkl. gesetzl. MwSt.,
Beschreibung
Produktdetails
Einband
Taschenbuch
Erscheinungsdatum
15.12.2011
Herausgeber
Ursula GresserVerlag
Springer BerlinSeitenzahl
182
Maße (L/B/H)
20.3/13.3/1.2 cm
Gewicht
231 g
Auflage
Softcover reprint of the original 1st ed. 1993
Sprache
Englisch
ISBN
978-3-642-84964-0
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.
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.
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