(Q40927942)

24 September 2017

title

Genetic fitness in Huntington's Disease and Spinocerebellar Ataxia 1: a population genetics model for CAG repeat expansions (English)

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24 September 2017

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spinocerebellar ataxia

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E Mantuano

10

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Liana Veneziano

object named as

L Veneziano

9

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Paola Giunti

object named as

P Giunti

7

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author name string

M Frontali

1

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24 September 2017

G Sabbadini

2

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24 September 2017

A Novelletto

3

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24 September 2017

C Jodice

4

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24 September 2017

F Naso

5

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24 September 2017

M Spadaro

6

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24 September 2017

A G Jacopini

8

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24 September 2017

P Malaspina

11

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24 September 2017

L Ulizzi

12

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24 September 2017

A Brice

13

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24 September 2017

A Durr

14

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24 September 2017

L Terrenato

15

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24 September 2017

language of work or name

English

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publication date

1 September 1996

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24 September 2017

published in

Annals of Human Genetics

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24 September 2017

volume

60

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24 September 2017

issue

Pt 5

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24 September 2017

page(s)

423-435

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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

24 September 2017

cites work

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-1809.1996.TB00440.X

Friedreich's ataxia: autosomal recessive disease caused by an intronic GAA triplet repeat expansion

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-1809.1996.TB00440.X

Evidence for a mechanism predisposing to intergenerational CAG repeat instability in spinocerebellar ataxia type I.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-1809.1996.TB00440.X

Length of uninterrupted CGG repeats determines instability in the FMR1 gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-1809.1996.TB00440.X

Epidemiological and linkage studies on Huntington's disease in Italy

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-1809.1996.TB00440.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-1809.1996.TB00440.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/10.1111%2FJ.1469-1809.1996.TB00440.X

CAG expansions in a novel gene for Machado-Joseph disease at chromosome 14q32.1

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-1809.1996.TB00440.X

Unstable expansion of CAG repeat in hereditary dentatorubral-pallidoluysian atrophy (DRPLA)

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-1809.1996.TB00440.X

Cryptic and polar variation of the fragile X repeat could result in predisposing normal alleles.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-1809.1996.TB00440.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-1809.1996.TB00440.X

Trinucleotide repeat expansion in neurological disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-1809.1996.TB00440.X

The Huntington's disease candidate region exhibits many different haplotypes

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-1809.1996.TB00440.X

De novo expansion of a (CAG)n repeat in sporadic Huntington's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-1809.1996.TB00440.X

Analysis of the trinucleotide repeat expansion in Italian families affected with Huntington disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-1809.1996.TB00440.X

Polymorphism analysis of the huntingtin gene in Italian families affected with Huntington disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-1809.1996.TB00440.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-1809.1996.TB00440.X

Mutational bias provides a model for the evolution of Huntington's disease and predicts a general increase in disease prevalence.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-1809.1996.TB00440.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-1809.1996.TB00440.X

Simple tandem DNA repeats and human genetic disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-1809.1996.TB00440.X

Changes of selection opportunities with a changing environment: regional heterogeneity in Italy

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-1809.1996.TB00440.X

A new polymerase chain reaction (PCR) assay for the trinucleotide repeat that is unstable and expanded on Huntington's disease chromosomes

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-1809.1996.TB00440.X

10.1111/J.1469-1809.1996.TB00440.X

21 January 2018

Identifiers

DOI

1 reference

24 September 2017

1 reference