Analysis of triplet repeat disorders

Analysis of triplet repeat disorders

by Hayden, Michael R. Rubinsztein, D. C., (David C.)

Type Book
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The clinical picture of diseases, caused by trinucleotide repeats, such as fragile X syndrome, myotonic dystrophy, Huntington's disease and forms of spinocerebella ataxia, provide the starting point for this authoritative review volume. The book proceeds to integrate the current understanding of the molecular pathologies of these diseases, their genotype-phenotype relationships, the mutational processes involved and the laboratory and clinical issues relating to genetic testing for these disord…

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Title Statements

  • Full title :Analysis of triplet repeat disorders / [edited by] D.C. Rubinsztein and M.R. Hayden.

Summary

The clinical picture of diseases, caused by trinucleotide repeats, such as fragile X syndrome, myotonic dystrophy, Huntington's disease and forms of spinocerebella ataxia, provide the starting point for this authoritative review volume. The book proceeds to integrate the current understanding of the molecular pathologies of these diseases, their genotype-phenotype relationships, the mutational processes involved and the laboratory and clinical issues relating to genetic testing for these disorders. Clinicians and researchers in genetics, neuroscience, pediatrics and psychiatry will all benefit from the comprehensive overviews contributed by recognized world experts.

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Edition Statements

  • Publication Date:1998.

Publication Statements

The Physical Object

  • Description:1 online resource (xvii, 327 pages : : illustrations.)

Edition Identifiers

  • ISBN:9780203887578, 0203887573
  • oclc:on1330994851
  • LC Classification:RB155.5
  • Dewey Decimal:616.042

Subjects

Chromosome Aberrations Fragile X Syndrome -- genetics Human molecular genetics Huntington Disease -- genetics Spinocerebellar Degenerations -- geneti… Trinucleotide Repeats -- genetics

Writers

Hayden, Michael R. Rubinsztein, D. C., (David C.)

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