(Q45290871)

11 December 2017

Relationship between trinucleotide repeat expansion and phenotypic variation in Huntington's disease (English)

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11 December 2017

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1

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11 December 2017

8

Gusella JF

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11 December 2017

MacMillan JC

2

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11 December 2017

Cheadle JP

3

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11 December 2017

Fenton I

4

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11 December 2017

Lazarou LP

5

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11 December 2017

Davies P

6

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11 December 2017

MacDonald ME

7

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11 December 2017

Harper PS

9

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11 December 2017

Shaw DJ

10

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11 December 2017

language of work or name

English

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publication date

1 August 1993

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11 December 2017

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11 December 2017

4

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11 December 2017

393-397

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11 December 2017

4

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https://scigraph.springernature.com/pub.10.1038/ng0893-393

11 December 2017

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cites work

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0893-393

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0893-393

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0893-393

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0893-393

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0893-393

7 January 2021

Huntington's Chorea in the Netherlands The problem of genetic heterogeneity

1 reference

https://api.crossref.org/works/10.1038%2FNG0893-393

7 January 2021

The natural history of Huntington disease: possible role of "aging genes".

1 reference

https://api.crossref.org/works/10.1038%2FNG0893-393

7 January 2021

Maternal transmission in Huntington's disease

1 reference

https://api.crossref.org/works/10.1038%2FNG0893-393

7 January 2021

Parental transmission in Huntington's disease

1 reference

https://api.crossref.org/works/10.1038%2FNG0893-393

7 January 2021

Patterns of inheritance of the symptoms of Huntington's disease suggestive of an effect of genomic imprinting

1 reference

https://api.crossref.org/works/10.1038%2FNG0893-393

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0893-393

7 January 2021

Detection of an unstable fragment of DNA specific to individuals with myotonic dystrophy

1 reference

https://api.crossref.org/works/10.1038%2FNG0893-393

7 January 2021

Factors influencing age at onset and duration of survival in Huntington's chorea

1 reference

https://api.crossref.org/works/10.1038%2FNG0893-393

7 January 2021

Non-random association between alleles detected at D4S95 and D4S98 and the Huntington's disease gene

1 reference

https://api.crossref.org/works/10.1038%2FNG0893-393

7 January 2021

Identifiers

DOI

10.1038/NG0893-393

1 reference

Dimensions Publication ID

11 December 2017

0 references

1 reference