ABI2

abl interactor 2
OMIM: 606442
PanelMode of inheritanceDetails
1 panel
R-numbers: R21, R412
Signed-off version 7.0
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
Intellectual disability, epilepsy, hypoplasia of the corpus callosum, and white matter abnormalities