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.