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Analysis of Triplet Repeat Disorders : Human Molecular Genetics - Michael Hayden

Analysis of Triplet Repeat Disorders

Human Molecular Genetics

By: Michael Hayden (Editor), David Rubinsztein (Editor)

Hardcover Published: 1st September 1998
ISBN: 9781859962664
Number Of Pages: 352

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Analysis of Triplet Repeat Disorders is aimed at clinicians and scientists who work with these diseases or who have an interest in the field. Using the clinical picture of these diseases as a starting point, the book reviews and integrates the current understanding of their molecular pathologies, the genotype-phenotype relationships, the mutational processes of trinucleotide repeats, and the laboratory and clinical issues relating to genetic testing for these disorders.

Foreword
Introduction
The Fraxa fragile site and fragile X syndrome
Molecular studies of the fragile sites Fraxe and Faxf
Myotonic dystrophy
Spinobulbar musculal atrophy
Polyglutamine tract vs protein context in SCA1 pathogenesis
Spinocerebellar ataxia type 2 (SCA2)
Spinocerebellar ataxia type 3/Machado Joseph disease
Spinocerebellar ataxia type 6 (SCA6)
Spinocerebellar ataxia type 7 (SCA7)
Huntingtons disease
Dentatorubral-pallidoluysian atrophy (DRLPA)
Friedrich's ataxia
Anticipation, triplet repeats and psychiatric disorders
Trinucleotide repeat mutation processes
Diagnostic testing for trinucleotide repeat diseases
Predictive testing for trinucleotide repeat diseases
Table of Contents provided by Publisher. All Rights Reserved.

ISBN: 9781859962664
ISBN-10: 1859962661
Series: Human Molecular Genetics
Audience: Professional
Format: Hardcover
Language: English
Number Of Pages: 352
Published: 1st September 1998
Publisher: GARLAND PUB
Country of Publication: GB
Dimensions (cm): 23.39 x 15.6  x 2.06
Weight (kg): 0.66
Edition Number: 1