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Description
Mutations in the genes encoding glycine decarboxylase and aminomethyltransferase are the most common causes of nonketotic hyperglycinemia (NKH), a severe genetic disorder characterized by high accumulation of glycine (Gly) in body fluids and tissues of patients [78]
Supports normal nervous system function*
43-H-SE 8/30/1943 2nd Lt
Tremellen, K
