Citations for
1SCDD, AASS
Identification of the alpha-Aminoadipic Semialdehyde Synthase Gene, Which Is Defective in Familial Hyperlysinemia.
Sacksteder KA, Biery BJ, Morrell JC, Goodman BK, Geisbrecht BV, Cox RP, Gould SJ, Geraghty MT.
Am J Hum Genet 66(6):1736-1743. 2000
2AASS, SCDD
Lysine degradation through the saccharopine pathway in mammals: involvement of both bifunctional and monofunctional lysine-degrading enzymes in mouse.
Papes F, Kemper EL, Cord-Neto G, Langone F, Arruda P.
Biochem J 344 Pt 2:555-63. 1999