NCAPD2

non-SMC condensin I complex subunit D2
OMIM: 615638
PanelMode of inheritanceDetails
1 panel
R-numbers: R88
Signed-off version 7.0
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Microcephaly 21, primary, autosomal recessive, OMIM:617983