DYNC1I2

dynein cytoplasmic 1 intermediate chain 2
OMIM: 603331
PanelMode of inheritanceDetails
1 panel
R-numbers: R88
Signed-off version 4.0
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Neurodevelopmental disorder with microcephaly and structural brain anomalies, OMIM:618492