The Expanding Role of MBD Genes in Autism: Identification of aMECP2Duplication and Novel Alterations inMBD5,MBD6, andSETDB1

Author:

Cukier Holly N.,Lee Joycelyn M.,Ma Deqiong,Young Juan I.,Mayo Vera,Butler Brittany L.,Ramsook Sandhya S.,Rantus Joseph A.,Abrams Alexander J.,Whitehead Patrice L.,Wright Harry H.,Abramson Ruth K.,Haines Jonathan L.,Cuccaro Michael L.,Pericak-Vance Margaret A.,Gilbert John R.

Publisher

Wiley

Subject

Genetics (clinical),Neurology (clinical),General Neuroscience

Reference77 articles.

1. A method and server for predicting damaging missense mutations;Adzhubei;Nature Methods,2010

2. The loss of methyl-CpG binding protein 1 leads to autism-like behavioral deficits;Allan;Human Molecular Genetics,2008

3. Systematic meta-analyses and field synopsis of genetic association studies in schizophrenia: The SzGene database;Allen;Nature Genetics,2008

4. American Psychiatric Association 1994 Diagnostic and statistical manual of mental disorders (DSM-IV) American Psychiatric Press, Inc. Washington

5. Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2;Amir;Nature Genetics,1999

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