Open AccessPM338. Investigation of the association of rare single nucleotide variants in methyl-CpG-binding domain protein 5 (MBD5) with phenotypes of autism spectrum disorders and schizophrenia.
Author(s) -
Kanako Ishizuka,
Branko Aleksić,
Chenyao Wang,
Hiroki Kimura,
Itaru Kushima,
Takashi Okada,
Norio Ozaki,
Yota Uno
Publication year - 2016
Publication title -
the international journal of neuropsychopharmacology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.897
H-Index - 107
eISSN - 1469-5111
pISSN - 1461-1457
DOI - 10.1093/ijnp/pyw041.338
Subject(s) - autism , phenotype , schizophrenia (object oriented programming) , association (psychology) , autism spectrum disorder , cpg site , genetics , single nucleotide polymorphism , medicine , psychology , biology , psychiatry , gene , genotype , dna methylation , psychotherapist , gene expression
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