A small homozygous microdeletion of 15q13.3 including the CHRNA7 gene in a girl with a spectrum of severe neurodevelopmental features
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Reference26 articles.
1. Microdeletion 15q13.3: A locus with incomplete penetrance for autism, mental retardation, and psychiatric disorders;Ben-Shachar;J Med Genet,2009
2. Increased sensitivity to nicotine-induced seizures in mice expressing the L250T alpha 7 nicotinic acetylcholine receptor mutation;Broide;Mol Pharmacol,2002
3. Familial and sporadic 15q13.3 microdeletions in idiopathic generalized epilepsy: Precedent for disorders with complex inheritance;Dibbens;Hum Mol Genet,2009
4. Homozygous loss of CHRNA7 on chromosome 15q13.3 causes severe encephalopathy with seizures and hypotonia;Endris;Am J Med Genet Part A,2010
5. Population-based and family-based association studies of an (AC)n dinucleotide repeat in alpha-7 nicotinic receptor subunit gene and schizophrenia;Fan;Schizophr Res,2006
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