Unstable Triplet Repeat Diseases-Reference-Cited by-同舟云学术

Unstable Triplet Repeat Diseases

Published:1995-01-15 Issue:2 Volume:91 Page:513-520
ISSN:0009-7322
Container-title:Circulation
language:en
Short-container-title:Circulation

Author:

Monckton Darren G.¹,Caskey C. Thomas¹

Affiliation:

1. From the Department of Molecular and Human Genetics, Howard Hughes Medical Institute and Human Genome Center, Baylor College of Medicine, Houston, Tex.

Abstract

Abstract Seven inherited human disorders are now associated with the intragenic expansion of triplet repeat DNA sequences. These repeats demonstrate extreme instability in both germline and somatic tissue, accounting for the unusual genetic inheritance patterns and symptom variability associated with these diseases.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Physiology (medical),Cardiology and Cardiovascular Medicine

Reference95 articles.

1. Mapping of DNA Instability at the Fragile X to a Trinucleotide Repeat Sequence P(CCG) n

2. Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome

3. Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradox

4. Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophy

5. Molecular basis of myotonic dystrophy: Expansion of a trinucleotide (CTG) repeat at the 3′ end of a transcript encoding a protein kinase family member

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