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Urinary iron excretion and renal metabolism of hemoglobin in hemolytic diseases

Epilepsy and movement disorders: A severe deficiency caused by rare mutations in the PNPO enzyme can result in encephalopathy, epilepsy, and movement disorders from infancy

Youll be advised on proper oral hygiene and a soft food diet during recovery

Data were presented as mean SEM

Biochemical Parameter Tests After collection of the serum and homogenization of the mouse livers, assay kits for alanine aminotransferase (ALT, #C009-2), aspartate transaminase (AST, #C010-2), TG (#A110-1), and cholesterol (CHO, #A111-1) from Nanjing Jiancheng Biotechnology Co., Ltd., Nanjing, China, were used to evaluate the corresponding biochemical parameters in 96-well plates (#701002, NEST Biotechnology, Wuxi, China) according to the instructions