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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)