SLC25A36

solute carrier family 25 member 36
OMIM: 616149
PanelMode of inheritanceDetails
1 panel
Component of the following Super Panels:
  • - Childhood onset leukodystrophy
Signed-off version 6.4
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Hyperinsulinemic hypoglycemia, familial, 8, OMIM:620211