Genetic fitness in Huntington's Disease and Spinocerebellar Ataxia 1: a population genetics model for CAG repeat expansions-Reference-Cited by-同舟云学术

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

Published:1996-09 Issue:5 Volume:60 Page:423-435
ISSN:0003-4800
Container-title:Annals of Human Genetics
language:en
Short-container-title:Ann Human Genet

Author:

FRONTALI M.,SABBADINI G.,NOVELLETTO A.,JODICE C.,NASO F.,SPADARO M.,GIUNTI P.,JACOPINI A. G.,VENEZIANO L.,MANTUANO E.,MALASPPNA P.,ULIZZI L.,BRICE A.,DURR A.,TERRENATO L.

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1469-1809.1996.tb00440.x/fullpdf

Reference39 articles.

1. Ancestral differences in the distribution of the Δ2642 glutamic acid polymorphism is associated with varying CAG repeat lengths on normal chromosomes: insights into the genetic evolution of Huntington disease

2. On the estimation of the age at onset distribution in Huntington's chorea using the EM algorithm

3. Friedreich's Ataxia: Autosomal Recessive Disease Caused by an Intronic GAA Triplet Repeat Expansion

4. Reply to “Meiotic drive and myotonic dystrophy”

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

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