(Q45289968)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12956863%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

title

Molecular analysis of Huntington's disease and linked polymorphisms in the Indian population (English)

1 reference

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7 November 2019

0 references

4

1 reference

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7 November 2019

author name string

Q Saleem

1

1 reference

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7 November 2019

S Roy

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12956863%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

U Murgood

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12956863%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

I C Verma

5

1 reference

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7 November 2019

A Anand

6

1 reference

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7 November 2019

U Muthane

7

1 reference

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7 November 2019

S Jain

8

1 reference

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7 November 2019

S K Brahmachari

9

1 reference

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7 November 2019

language of work or name

English

0 references

publication date

1 October 2003

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12956863%20AND%20SRC:MED&resulttype=core&format=json

Acta Neurologica Scandinavica

7 November 2019

published in

1 reference

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7 November 2019

volume

108

1 reference

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7 November 2019

issue

4

1 reference

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7 November 2019

page(s)

281-286

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12956863%20AND%20SRC:MED&resulttype=core&format=json

Trinucleotide instability: a repeating theme in human inherited disorders

7 November 2019

cites work

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0404.2003.00133.X

Analysis of a very large trinucleotide repeat in a patient with juvenile Huntington's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0404.2003.00133.X

Close associations between prevalences of dominantly inherited spinocerebellar ataxias with CAG-repeat expansions and frequencies of large normal CAG alleles in Japanese and Caucasian populations

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0404.2003.00133.X

The diagnosis of Huntington's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0404.2003.00133.X

A clinical study of patients with genetically confirmed Huntington's disease from India

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0404.2003.00133.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0404.2003.00133.X

Expanding colonies and expanding repeats

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0404.2003.00133.X

Molecular analysis of autosomal dominant hereditary ataxias in the Indian population: high frequency of SCA2 and evidence for a common founder mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0404.2003.00133.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0404.2003.00133.X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0404.2003.00133.X

7 January 2021

Simple repetitive sequences in the genome: structure and functional significance

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0404.2003.00133.X

7 January 2021

Huntington's disease in Chinese: a hypothesis of its origin

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0404.2003.00133.X

7 January 2021

Prevalence of Huntington's disease among UK immigrants from the Indian subcontinent

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0404.2003.00133.X

7 January 2021

DNA haplotype analysis of Huntington disease reveals clues to the origins and mechanisms of CAG expansion and reasons for geographic variations of prevalence

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0404.2003.00133.X

7 January 2021

Unified Huntington's disease rating scale: Reliability and consistency

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0404.2003.00133.X

7 January 2021

A simple salting out procedure for extracting DNA from human nucleated cells

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0404.2003.00133.X

7 January 2021

Analysis of the huntingtin gene reveals a trinucleotide-length polymorphism in the region of the gene that contains two CCG-rich stretches and a correlation between decreased age of onset of Huntington's disease and CAG repeat number

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0404.2003.00133.X

7 January 2021

A CCG repeat polymorphism adjacent to the CAG repeat in the Huntington disease gene: implications for diagnostic accuracy and predictive testing

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0404.2003.00133.X

7 January 2021

Structure and expression of the Huntington's disease gene: evidence against simple inactivation due to an expanded CAG repeat

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0404.2003.00133.X

7 January 2021

A dinucleotide repeat polymorphism at the D4S127 locus

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0404.2003.00133.X

7 January 2021

Haplotype analysis of the delta 2642 and (CAG)n polymorphisms in the Huntington's disease (HD) gene provides an explanation for an apparent 'founder' HD haplotype

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0404.2003.00133.X

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/10.1034%2FJ.1600-0404.2003.00133.X

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/10.1034%2FJ.1600-0404.2003.00133.X

7 January 2021