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

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B Kremer

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H Telenius

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J Theilmann

5

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E Starr

7

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B Lin

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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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publication date

August 1993

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language of work or name

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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

21 January 2018

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7 January 2021

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

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7 January 2021

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

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7 January 2021

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

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7 January 2021

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

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7 January 2021

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

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7 January 2021

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

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7 January 2021

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

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7 January 2021

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

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7 January 2021

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

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7 January 2021

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

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