Mutations in the chromatin-associated protein ATRX-Reference-Cited by-同舟云学术

Mutations in the chromatin-associated protein ATRX

Published:2008-06 Issue:6 Volume:29 Page:796-802
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Hum. Mutat.

Author:

Gibbons Richard J.,Wada Takahito,Fisher Christopher A.,Malik Nicola,Mitson Matthew J.,Steensma David P.,Fryer Alan,Goudie David R.,Krantz Ian D.,Traeger-Synodinos Joanne

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference33 articles.

1. Carpenter-Waziri syndrome results from a mutation in XNP;Abidi;Am J Med Genet,1999

2. Mutation in the 5′ alternatively spliced region of the XNP/ATR-X gene causes Chudley-Lowry syndrome;Abidi;Eur J Hum Genet,2005

3. Structural consequences of disease-causing mutations in the ATRX-DNMT3-DNMT3L (ADD) domain of the chromatin-associated protein ATRX;Argentaro;Proc Natl Acad Sci USA,2007

4. Mutations in PHD-like domain of the ATRX gene correlate with severe psychomotor impairment and severe urogenital abnormalities in patients with ATRX syndrome;Badens;Clin Genet,2006

5. ATRX syndrome in a girl with a heterozygous mutation in the ATRX Zn finger domain and a totally skewed X-inactivation pattern;Badens;Am J Med Genet A,2006

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