Shanti, N.D.; Shashikumar, K.C.; Desai, P.V.
(Neurochemical Research. 29(12); 2004; 2197-2206.)
Hyperprolinemia type II ( HPII) is an autosomal recessive disorder caused by the severe deficiency of enzyme Delta(1)-pyrroline-5-carboxylic acid dehydrogenase leading to tissue accumulation of proline. Chronic administration ...