The relationship between trinucleotide (CAG) repeat length and clinical features of Huntington's disease (Q28264134)

8

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author name string

S E Andrew

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Y P Goldberg

2

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B Kremer

3

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H Telenius

4

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J Theilmann

5

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E Starr

7

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B Lin

9

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M A Kalchman

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

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language of work or name

English

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publication date

August 1993

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published in

Nature Genetics

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volume

4

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issue

4

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page(s)

398-403

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cites work

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

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Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1.

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Dynamic mutations: a new class of mutations causing human disease

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Questions of expansion

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A polymorphic DNA marker genetically linked to Huntington's disease

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A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes.

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

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

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An unstable triplet repeat in a gene related to myotonic muscular dystrophy

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Relationship between parental trinucleotide GCT repeat length and severity of myotonic dystrophy in offspring

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Correlation between CTG trinucleotide repeat length and frequency of severe congenital myotonic dystrophy

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The correlation of age of onset with CTG trinucleotide repeat amplification in myotonic dystrophy

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

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Analysis of human Y-chromosome-specific reiterated DNA in chromosome variants

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

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