ARHGAP19

Rho GTPase activating protein 19
OMIM: 611587
PanelMode of inheritanceDetails
1 panel
R-numbers: R78
Signed-off version 8.30
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
motor peripheral neuropathy, MONDO:0002316, Charcot-Marie-Tooth disease, axonal, type 2KK, OMIM:621466