Condition: CATARACT 32, MULTIPLE TYPES
rs1553630279 in
CTNNB1 gene and
CATARACT 32, MULTIPLE TYPES
PMID 27915094 2017 Clinical features associated with CTNNB1 de novo loss of function mutations in ten individuals.
PMID 24668549 2014 A new intellectual disability syndrome caused by CTNNB1 haploinsufficiency.
PMID 2614104 1989 [Intraoperative echocardiographic assessment of left ventricular muscle volume changes after intracardiac operation under cardiopulmonary bypass].