Malformations of cortical developmentGene: ERMARD
Possible DD on G2P. Only reported in one family
Created: 19 Dec 2016, 11:39 a.m.
Mode of inheritance
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Periventricular nodular heterotopia 6 615544
This gene has been classified as Red List (Low Evidence).
ERMARD was added to Malformations of cortical developmentpanel. Sources: UKGTN
ERMARD was created by agardham