Correlation between CTG trinucleotide repeat length and frequency of severe congenital myotonic dystrophy (Q34231790)

31 July 2017

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

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31 July 2017

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Tsilfidis C

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31 July 2017

MacKenzie AE

2

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31 July 2017

Mettler G

3

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31 July 2017

Barceló J

4

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31 July 2017

Korneluk RG

5

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31 July 2017

language of work or name

English

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publication date

1 June 1992

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31 July 2017

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31 July 2017

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31 July 2017

192-195

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31 July 2017

3

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https://scigraph.springernature.com/pub.10.1038/ng0692-192

31 July 2017

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cites work

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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https://api.crossref.org/works/10.1038%2FNG0692-192

Cloning of the essential myotonic dystrophy region and mapping of the putative defect

21 January 2018

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https://api.crossref.org/works/10.1038%2FNG0692-192

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

21 January 2018

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https://api.crossref.org/works/10.1038%2FNG0692-192

Expansion of an unstable DNA region and phenotypic variation in myotonic dystrophy

21 January 2018

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https://api.crossref.org/works/10.1038%2FNG0692-192

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

21 January 2018

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https://api.crossref.org/works/10.1038%2FNG0692-192

Structure and function of telomeres

21 January 2018

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https://api.crossref.org/works/10.1038%2FNG0692-192

Dystrophia myotonica in childhood

21 January 2018

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https://api.crossref.org/works/10.1038%2FNG0692-192

7 January 2021

Congenital myotonic dystrophy in Britain. I. Clinical aspects

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https://api.crossref.org/works/10.1038%2FNG0692-192

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0692-192

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0692-192

7 January 2021

Instability of a 550-base pair DNA segment and abnormal methylation in fragile X syndrome

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https://api.crossref.org/works/10.1038%2FNG0692-192

7 January 2021

Fragile X genotype characterized by an unstable region of DNA.

1 reference

https://api.crossref.org/works/10.1038%2FNG0692-192

7 January 2021

Incidence, severity, and time-course of motoneurone dysfunction in myotonic dystrophy: their significance for an understanding of anticipation

1 reference

https://api.crossref.org/works/10.1038%2FNG0692-192

7 January 2021

Anticipation in myotonic dystrophy: fact or fiction?

1 reference

https://api.crossref.org/works/10.1038%2FNG0692-192

7 January 2021

Congenital myotonic dystrophy in Britain. II. Genetic basis

1 reference

https://api.crossref.org/works/10.1038%2FNG0692-192

7 January 2021

Genealogical reconstruction of myotonic dystrophy in the Saguenay-Lac-Saint-Jean area (Quebec, Canada)

1 reference

https://api.crossref.org/works/10.1038%2FNG0692-192

7 January 2021

Criteria for establishing the validity of genetic recombination in myotonic dystrophy

1 reference

https://api.crossref.org/works/10.1038%2FNG0692-192

7 January 2021

Identifiers

DOI

10.1038/NG0692-192

1 reference

31 July 2017

1 reference