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V.AgarwalN.et al (2008)

In its acetylated form this residue is associated with active transcription (Wang et al., 2008)

5-oxoprolinase deficiency due to OPLAH gene mutation on chromosome 8q24.3 is a benign biochemical disorder of the gamma-glutamyl cycle that is transmitted as an autosomal recessive trait (04
Matijasic BB, Obermajer T, Lipoglavsek L, Grabnar I, Avgustin G, Rogelj I

from the University of Kentucky under the supervision of Prof
