ARX polyalanine expansions are highly implicated in familial cases of mental retardation with infantile epilepsy and/or hand dystonia-Reference-Cited by-同舟云学术

ARX polyalanine expansions are highly implicated in familial cases of mental retardation with infantile epilepsy and/or hand dystonia

Published:2010-12-28 Issue:1 Volume:155 Page:98-105
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Cossée Mireille,Faivre Laurence,Philippe Christophe,Hichri Heifa,de Saint-Martin Anne,Laugel Vincent,Bahi-Buisson Nadia,Lemaitre Jean-François,Leheup Bruno,Delobel Bruno,Demeer Bénédicte,Poirier Karine,Biancalana Valérie,Pinoit Jean-Michel,Julia Sophie,Chelly Jamel,Devys Didier,Mandel Jean-Louis

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.33785/fullpdf

Reference26 articles.

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3. ARX, a novel Prd-class-homeobox gene highly expressed in the telencephalon, is mutated in X-linked mental retardation;Bienvenu;Hum Mol Genet,2002

4. An assay for X inactivation based on differential methylation at the fragile X locus, FMR1;Carrel;Am J Med Genet,1996

5. Mutation frequencies of X-linked mental retardation genes in families from the EuroMRX consortium;De Brouwer;Hum Mutat,2007

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