|
Books > Medicine > General issues > Medical equipment & techniques > Medical research
|
Buy Now
Molecular Genetics, Biochemistry and Clinical Aspects of Inherited Disorders of Purine and Pyrimidine Metabolism (Paperback, Softcover reprint of the original 1st ed. 1993)
Loot Price: R2,745
Discovery Miles 27 450
|
|
|
Molecular Genetics, Biochemistry and Clinical Aspects of Inherited Disorders of Purine and Pyrimidine Metabolism (Paperback, Softcover reprint of the original 1st ed. 1993)
Expected to ship within 10 - 15 working days
|
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.
General
Is the information for this product incomplete, wrong or inappropriate?
Let us know about it.
Does this product have an incorrect or missing image?
Send us a new image.
Is this product missing categories?
Add more categories.
Review This Product
No reviews yet - be the first to create one!
|
|
Email address subscribed successfully.
A activation email has been sent to you.
Please click the link in that email to activate your subscription.
Welcome to Loot.co.za!
Sign in / Register |Wishlists & Gift Vouchers |Help | Advanced search
