Share
molecular genetics, biochemistry and clinical aspects of inherited disorders of purine and pyrimidine metabolism
Ursula Gresser
(Illustrated by)
·
R. a. De Abreu
(Contributions by)
·
J. Aimi
(Contributions by)
·
Springer
· Paperback
molecular genetics, biochemistry and clinical aspects of inherited disorders of purine and pyrimidine metabolism - Gresser, Ursula ; Abreu, R. a. De ; Aimi, J.
Choose the list to add your product or create one New List
✓ Product added successfully to the Wishlist.
Go to My Wishlists
Origin: U.S.A.
(Import costs included in the price)
It will be shipped from our warehouse between
Wednesday, August 07 and
Wednesday, August 14.
You will receive it anywhere in United Kingdom between 1 and 3 business days after shipment.
Synopsis "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.