Molecular Genetics, Biochemistry and Clinical Aspects of Inherited Disorders of Purine and Pyrimidine Metabolism
Author:   U Gresser ,  Ursula Gresser
Publisher:   Springer
ISBN:  

9780387567747


Pages:   182
Publication Date:   01 January 1993
Format:   Undefined
Availability:   Out of stock   Availability explained


Our Price $361.68 Quantity:  
Add to Cart

Share |

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


Overview

Inherited disorders of purine and pyrimidine metabolism in man lead to severe diseases. At the 2nd Muenchner Adventssymposium, the genetic basis, clinical aspects and the biochemical basis of the following diseases was discussed: Hypoxanthine phosphoribosyltransferase deficiency (HGPRT-deficiency), adenine phosphoribosyltransferase deficiency (APRT-deficiency), hyperuricemia and gout, adenosine deaminase deficiency (ADA-deficiency, and purine nucleoside phosphorylase deficiency (PNP-deficiency).

Full Product Details

Author:   U Gresser ,  Ursula Gresser
Publisher:   Springer
Imprint:   Springer
ISBN:  

9780387567747


ISBN 10:   0387567747
Pages:   182
Publication Date:   01 January 1993
Audience:   General/trade ,  General
Format:   Undefined
Publisher's Status:   Unknown
Availability:   Out of stock   Availability explained

Table of Contents

Reviews

Author Information

Tab Content 6

Author Website:  

Countries Available

All regions
Latest Reading Guide

April RG 26_2

 

Shopping Cart
Your cart is empty
 Shopping cart
Mailing List

 

Sign up now