SCHAD
MIM.601609 4q22-q26
Function
mitochondrial fatty acid oxidation
Pathology
SCHAD deficiency (MIM.601609)
mutations in congenital hyperinsulinism (familial hyperinsulinemic hypoglycemia)
Function
mitochondrial fatty acid oxidation
Pathology
SCHAD deficiency (MIM.601609)
mutations in congenital hyperinsulinism (familial hyperinsulinemic hypoglycemia)
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