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The relationship between trinucleotide (CAG) repeat length and clinical features of Huntington's disease

Author

Shelin Adam

Ferdinando Squitieri

published in: Nature Genetics

date of publication: 1993-08

language: angla lingvo

main subject: malsano de Huntington

Bibliographic databases:

Cites articles 17

Date

Title

Authors

1977-03-01

Analysis of human Y-chromosome-specific reiterated DNA in chromosome variants
1983-11-01

A polymorphic DNA marker genetically linked to Huntington's disease
1991-12-20

Variation of the CGG repeat at the fragile X site results in genetic instability: resolution of the Sherman paradox,Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradox
1991-07-01

Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophy
1991-06-01

Mapping of DNA instability at the fragile X to a trinucleotide repeat sequence p(CCG)n
1992-02-01

Molecular basis of myotonic dystrophy: expansion of a trinucleotide (CTG) repeat at the 3' end of a transcript encoding a protein kinase family member
1992-09-01

Dynamic mutations: a new class of mutations causing human disease
1992-03-01

Myotonic dystrophy mutation: an unstable CTG repeat in the 3' untranslated region of the gene
1992-03-01

An unstable triplet repeat in a gene related to myotonic muscular dystrophy
1992-06-01

Correlation between CTG trinucleotide repeat length and frequency of severe congenital myotonic dystrophy
1992-11-01

The correlation of age of onset with CTG trinucleotide repeat amplification in myotonic dystrophy
1992-12-01

Meiotic stability and genotype-phenotype correlation of the trinucleotide repeat in X-linked spinal and bulbar muscular atrophy
1993-07-01

Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1.
1993-05-01

Questions of expansion
1993-03

A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes
1993-04-01

Relationship between parental trinucleotide GCT repeat length and severity of myotonic dystrophy in offspring
1993-06-01

A PCR method for accurate assessment of trinucleotide repeat expansion in Huntington disease

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