J. Wilson

Ataxia associated with increased plasma concentrations of pristanic acid, phytanic acid and C27 bile acids but normal fibroblast branched-chain fatty acid oxidation

K. Mills, P. Clayton, G. Mannaerts, 1996, Journal of Inherited Metabolic Disease.

Absence of hepatic molybdenum cofactor: An inborn error of metabolism leading to a combined deficiency of sulphite oxidase and xanthine dehydrogenase

M. Durán, K. Rajagopalan, J. Johnson, 1983, Journal of Inherited Metabolic Disease.

Hepatic fatty acid synthase gene transcription is induced by a dietary copper deficiency.

S. Clarke, R. Baillie, K. Allen, 1997, The American journal of physiology.

Isolated dihydroxyacetonephosphate acyltransferase deficiency presenting with developmental delay

R. Wanders, R. Schutgens, P. Clayton, 1994, Journal of Inherited Metabolic Disease.