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References OMIM Gene GeneReviews HGMD HGNC
GENATLAS PHENOTYPE
last update : 19-10-2015
Symbol MRD19
Location 3p22.1
Name mental retardation, autosomal dominant 19
Corresponding gene CTNNB1
Genetic determination autosomal dominant
Function/system disorder mental retardation
Type disease
Remark(s)