Condition: MENTAL RETARDATION, AUTOSOMAL DOMINANT 19


rs1553630279 in CTNNB1 gene and MENTAL RETARDATION, AUTOSOMAL DOMINANT 19 PMID 2614104 1989 [Intraoperative echocardiographic assessment of left ventricular muscle volume changes after intracardiac operation under cardiopulmonary bypass].

PMID 24668549 2014 A new intellectual disability syndrome caused by CTNNB1 haploinsufficiency.

PMID 27915094 2017 Clinical features associated with CTNNB1 de novo loss of function mutations in ten individuals.