Kure S; Kato K; Dinopoulos A; Gail C; DeGrauw TJ; Christodoulou J; Bzduch V; Kálmánchey, Rozália; Fekete, György; Trojovsky A; Plecko B; Breningstall G; Tohyama J; Aoki Y; Matsubara Y
(2006)
Nonketotic hyperglycinemia (NKH) is an inborn error of metabolism characterized by accumulation of glycine in body fluids and various neurological symptoms. NKH is caused by deficiency of the glycine cleavage multi-enzyme ...