(Q45290275)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8252043%20AND%20SRC:MED&resulttype=core&format=json

28 October 2019

title

Molecular analysis of new mutations for Huntington's disease: intermediate alleles and sex of origin effects (English)

1 reference

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28 October 2019

0 references

1 reference

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28 October 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8252043%20AND%20SRC:MED&resulttype=core&format=json

28 October 2019

Goldberg YP

1 reference

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28 October 2019

Kremer B

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8252043%20AND%20SRC:MED&resulttype=core&format=json

28 October 2019

Andrew SE

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8252043%20AND%20SRC:MED&resulttype=core&format=json

28 October 2019

Theilmann J

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8252043%20AND%20SRC:MED&resulttype=core&format=json

28 October 2019

Graham RK

1 reference

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28 October 2019

Telenius H

1 reference

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28 October 2019

Sajoo A

1 reference

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28 October 2019

Starr E

1 reference

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28 October 2019

language of work or name

English

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publication date

1 October 1993

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28 October 2019

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28 October 2019

volume

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28 October 2019

issue

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28 October 2019

page(s)

174-179

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

28 October 2019

cites work

1 reference

https://api.crossref.org/works/10.1038%2FNG1093-174

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG1093-174

7 January 2021

New mutation to Huntington's disease

1 reference

https://api.crossref.org/works/10.1038%2FNG1093-174

7 January 2021

Huntington's chorea arising as a fresh mutation

1 reference

https://api.crossref.org/works/10.1038%2FNG1093-174

7 January 2021

Mutation in Huntington's chorea

1 reference

https://api.crossref.org/works/10.1038%2FNG1093-174

7 January 2021

The Huntington's disease candidate region exhibits many different haplotypes

1 reference

https://api.crossref.org/works/10.1038%2FNG1093-174

7 January 2021

DNA analysis of distinct populations suggests multiple origins for the mutation causing Huntington disease

1 reference

https://api.crossref.org/works/10.1038%2FNG1093-174

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG1093-174

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG1093-174

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%2FNG1093-174

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG1093-174

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%2FNG1093-174

7 January 2021

Intergenerational stability of the myotonic dystrophy protomutation

1 reference

https://api.crossref.org/works/10.1038%2FNG1093-174

7 January 2021

Retreat of the triplet repeat?

1 reference

https://api.crossref.org/works/10.1038%2FNG1093-174

7 January 2021

Parental age and mutation

1 reference

https://api.crossref.org/works/10.1038%2FNG1093-174

7 January 2021

Parental age effects on the occurrence of new mutations for the Marfan syndrome

1 reference

https://api.crossref.org/works/10.1038%2FNG1093-174

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG1093-174

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG1093-174

7 January 2021

Identifiers

DOI

10.1038/NG1093-174

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8252043%20AND%20SRC:MED&resulttype=core&format=json

Dimensions Publication ID

28 October 2019

1005018725

0 references

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8252043%20AND%20SRC:MED&resulttype=core&format=json