LOS ANGELES--(BUSINESS WIRE)--ChromaDex Corp. (NASDAQ: CDXC) today announced a new research initiative with the Citrin Foundation of Singapore to study the effects of Niagen® nicotinamide riboside (NR ...
Mutations in SLC25A13 cause citrin deficiency, which has three phenotypes: neonatal intrahepatic cholestasis caused by citrin deficiency (NICCD), failure to thrive and dyslipidemia caused by citrin ...
Scientists at City of Hope have unraveled how citrin deficiency (CD), a rare genetic disorder that prevents the liver from converting food into energy efficiently, can trigger fat buildup in the liver ...
(HealthDay News) — The clinical features of citrin deficiency (CD) may mimic those of anorexia nervosa (AN), according to a case report published online July 20 in Pediatrics. Satsuki Takeuchi, MD, ...
ChromaDex External Research Program (CERP) and the Citrin Foundation to collaborate on series of studies exploring rare disease citrullinemia Citrin deficiency is a rare genetic condition that may ...
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