MME

membrane metalloendopeptidase
OMIM: 120520
PanelMode of inheritanceDetails
1 panel
R-numbers: R78
Signed-off version 2.1
BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Phenotypes
Charcot-Marie-Tooth disease, axonal, type 2T, OMIM:617017