A new single gene deletion on 2q34:ERBB4is associated with intellectual disability
Author:
Affiliation:
1. Faculty of Medicine, Department of Human and Medical Genetics; Vilnius University; Vilnius; Lithuania
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.35911/fullpdf
Reference14 articles.
1. Early myoclonic encephalopathy caused by a disruption of the neuregulin-1 receptor ErbB4;Backx;Eur J Hum Genet,2009
2. Neuregulin 1-erbB4 pathway in schizophrenia: From genes to an interactome;Banerjee;Brain Res Bull,2010
3. Aberrant neural and cardiac development in mice lacking the erbB4 neuregulin receptor;Gassman;Nature,1995
4. Heregulin, but not ErbB2 or ErbB3, heterozygous mutant mice exhibit hyperactivity in multiple behavioral tasks;Gerlai;Behav Brain Res,2000
5. Behavioral characteristics of a nervous system-specific erbB4 knock-out mouse;Golub;Behav Brain Res,2004
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