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

Editors: Gresser, Ursula (Ed.)

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Table of contents (24 chapters)

  • Introductory Remarks

    Watts, R. W. E.

    Pages 3-4

  • The Clinical Aspects of HGPRT Deficiency

    Kamilli, I. (et al.)

    Pages 5-11

  • The Biochemical Basis of HGPRT Deficiency

    Puig, J. G. (et al.)

    Pages 12-26

  • Prenatal Diagnosis of Lesch-Nyhan Syndrome

    Mateos, F. A. (et al.)

    Pages 27-32

  • The Genetic Basis of HGPRT Deficiency

    Davidson, B. L. (et al.)

    Pages 33-40

Buy this book

eBook $119.00
price for USA in USD (gross)
  • ISBN 978-3-642-84962-6
  • Digitally watermarked, DRM-free
  • Included format: PDF
  • ebooks can be used on all reading devices
  • Immediate eBook download after purchase
Softcover $159.99
price for USA in USD
  • ISBN 978-3-642-84964-0
  • Free shipping for individuals worldwide
  • Usually dispatched within 3 to 5 business days.
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Bibliographic Information

Bibliographic Information
Book Title
Molecular Genetics, Biochemistry and Clinical Aspects of Inherited Disorders of Purine and Pyrimidine Metabolism
Editors
  • Ursula Gresser
Copyright
1993
Publisher
Springer-Verlag Berlin Heidelberg
Copyright Holder
Springer Verlag, Berlin Heidelberg
eBook ISBN
978-3-642-84962-6
DOI
10.1007/978-3-642-84962-6
Softcover ISBN
978-3-642-84964-0
Edition Number
1
Number of Pages
XIV, 182
Topics