Concentration Details

Metabolite
HMDB0000904 (Citrulline)
Biospecimen
Blood
Status
Detected and Quantified
Data source
Referenced
Concentration
3-5 uM
Age
Children (1-13 years old)
Sex
Male
Condition
Narp Syndrome
References
    1. Parfait B, de Lonlay P, von Kleist-Retzow JC, Cormier-Daire V, Chretien D, Rotig A, Rabier D, Saudubray JM, Rustin P, Munnich A: The neurogenic weakness, ataxia and retinitis pigmentosa (NARP) syndrome mtDNA mutation (T8993G) triggers muscle ATPase deficiency and hypocitrullinaemia. Eur J Pediatr. 1999 Jan;158(1):55-8. [PubMed:9950309 ]