Confirmation of an ARID2 defect in SWI/SNF-related intellectual disability-Reference-Cited by-同舟云学术

Confirmation of an ARID2 defect in SWI/SNF-related intellectual disability

Published:2017-09-08 Issue:11 Volume:173 Page:3104-3108
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am J Med Genet

Author:

Van Paemel Ruben¹,De Bruyne Pauline²,van der Straaten Saskia³,D'hondt Marleen²,Fränkel Urlien⁴,Dheedene Annelies¹,Menten Björn¹,Callewaert Bert¹^ORCID

Affiliation:

1. Center for Medical Genetics; Ghent University Hospital; Ghent Belgium

2. Department of Pediatric Gastroenterology; Ghent University Hospital; Ghent Belgium

3. Department of Pediatric Endocrinology; Ghent University Hospital; Ghent Belgium

4. Center for Developmental Disorders; Ghent University Hospital; Ghent Belgium

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference16 articles.

1. Heterozygous missense mutations in SMARCA2 cause nicolaides-baraitser syndrome;Houdt;Nature Genetics,2012

2. Clinical correlations of mutations affecting six components of the SWI/SNF complex: Detailed description of 21 patients and a review of the literature;Kosho;American Journal of Medical Genetics Part A,2013

3. SMARCA2 and other genome-wide supported schizophrenia-associated genes: Regulation by REST/NRSF, network organization and primate-specific evolution;Loe-Mie;Human Molecular Genetics,2010

4. A specificity and targeting subunit of a human SWI/SNF family-related chromatin-remodeling complex;Nie;Molecular and Cellular Biology,2000

5. DNA-binding properties of ARID family proteins;Patsialou;Nucleic Acids Research,2005

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