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GENATLAS PHENOTYPE

last update : 07-11-2013

Symbol	MRD6
Location	12p13.1
Name	mental retardation, autosomal dominant 6
Corresponding gene	GRIN2B
Main clinical features	mild to moderate mental retardation, behavioral anomalies, and abnormal electroencephalogram (EEG)
Genetic determination	autosomal dominant
Function/system disorder	mental retardation
Type	disease

Remark(s)