L.T.K. Wong

Carnitine transporter defect due to a novel mutation in the SLC22A5 gene presenting with peripheral neuropathy

N. Longo, P. Waters, M. Pasquali, 2004, Journal of Inherited Metabolic Disease.

The High Incidence of Valproate Hepatotoxicity in Infants May Relate to Familial Metabolic Defects

J. Dimmick, D. Applegarth, A. Davidson, 1990, Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques.

Orthotopic liver transplantation in a patient with carbamyl phosphate synthetase deficiency and cystic fibrosis.

C. Scudamore, U. Steinbrecher, S. Sirrs, 2003, Paediatrics & child health.