A common SNP haplotype provides molecular proof of a founder effect of Huntington disease linking two South African populations. (Q45304302)

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26 December 2019

title

A common SNP haplotype provides molecular proof of a founder effect of Huntington disease linking two South African populations (English)

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26 December 2019

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26 December 2019

author name string

Jacquie Greenberg

series ordinal

2

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26 December 2019

publication date

28 February 2007

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European Journal of Human Genetics

26 December 2019

published in

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26 December 2019

volume

15

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26 December 2019

issue

5

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26 December 2019

page(s)

590-595

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Diagnosis of Huntington Disease

26 December 2019

cites work

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201796

7 January 2021

Ancient origin of the CAG expansion causing Huntington disease in a Spanish population.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201796

7 January 2021

Ancestral differences in the distribution of the delta 2642 glutamic acid polymorphism is associated with varying CAG repeat lengths on normal chromosomes: insights into the genetic evolution of Huntington disease

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201796

7 January 2021

A single allele from the polymorphic CCG rich sequence immediately 3' to the unstable CAG trinucleotide in the IT15 cDNA shows almost complete disequilibrium with Huntington's disease chromosomes in the Scottish population

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201796

7 January 2021

Linkage disequilibrium between the expanded (CAG)n repeat and an allele of the adjacent (CCG)n repeat in Huntington's disease patients of Greek origin.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201796

7 January 2021

Analysis of CAG and CCG repeats in Huntingtin gene among HD patients and normal populations of India

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201796

7 January 2021

Analysis of triplet repeats in the huntingtin gene in Japanese families affected with Huntington's disease

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201796

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%2FSJ.EJHG.5201796

7 January 2021

Genetic linkage between Huntington disease and the D4S10 locus in South African families: further evidence against non-allelic heterogeneity

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201796

7 January 2021

Two buffer PAGE system-based SSCP/HD analysis: a general protocol for rapid and sensitive mutation screening in cystic fibrosis and any other human genetic disease

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201796

7 January 2021

Allelic discrimination by denaturing high-performance liquid chromatography

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201796

7 January 2021

Detection of mutations in the dystrophin gene via automated DHPLC screening and direct sequencing

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201796

7 January 2021

Faster haplotype frequency estimation using unrelated subjects.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201796

7 January 2021

New tools for preimplantation genetic diagnosis of Huntington's disease and their clinical applications

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201796

7 January 2021

Identifiers

DOI

10.1038/SJ.EJHG.5201796

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17327878%20AND%20SRC:MED&resulttype=core&format=json

Dimensions Publication ID

26 December 2019

1048784142

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