ARL3

ADP ribosylation factor like GTPase 3
OMIM: 604695
PanelMode of inheritanceDetails
1 panel
R-numbers: R32
Signed-off version 3.3
BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Phenotypes
Joubert syndrome 35, OMIM:61816, cone-rod dystrophy, MONDO:0015993, Retinitis pigmentosa 83, OMIM:618173