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Ataxia-Telangiectasia

  • Conference proceedings
  • © 1993

Overview

Part of the book series: Nato ASI Subseries H: (ASIH, volume 77)

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Table of contents (23 papers)

  1. Introduction

  2. Isolation of A-T Gene(s)

  3. A-T Heterozygotes and Complementation

Keywords

About this book

Ataxia-telangiectasia or A-T is a fatal progressive neurological disease of children. The symptoms indicate disruptions in the development of such diverse body parts as cerebellum, thymus and chromosomes. The patients are unduly sensitive to ionizing radiation, immunodeficient, and a third of them develops cancer. All of this stems from defects of a single gene. Provided here is an up-to-date review of all important work in thefield. A wide spectrum of topics is covered, namely genetics, chromosome 11 mapping, radiobiology, complementation, heterozygote identification, clinical variants, biochemistry, and treatment of A-T.

Editors and Affiliations

  • Department of Pathology, University of California Los Angeles School of Medicine, Los Angeles, USA

    Richard A. Gatti

  • Laboratory of Radiobiology and Environmental Health, University of California San Francisco, San Francisco, USA

    Robert B. Painter

Bibliographic Information

  • Book Title: Ataxia-Telangiectasia

  • Editors: Richard A. Gatti, Robert B. Painter

  • Series Title: Nato ASI Subseries H:

  • DOI: https://doi.org/10.1007/978-3-642-78278-7

  • Publisher: Springer Berlin, Heidelberg

  • eBook Packages: Springer Book Archive

  • Copyright Information: Springer-Verlag Berlin Heidelberg 1993

  • Softcover ISBN: 978-3-642-78280-0Published: 23 June 2012

  • eBook ISBN: 978-3-642-78278-7Published: 29 June 2013

  • Series ISSN: 1010-8793

  • Edition Number: 1

  • Number of Pages: XXIII, 283

  • Number of Illustrations: 18 b/w illustrations

  • Topics: Pathology, Human Genetics, Oncology, Immunology, Cancer Research

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