Smith, Robert L.

Missense mutation in flavin-containing mono-oxygenase 3 gene, FMO3, underlies fish-odour syndrome

Dolphin, C. T., Janmohamed, A., Smith, R. L., Shephard, E. A., & Phillips, L. R. (1997) · Nature Genetics

Pharmacogenetics and Drug MetabolismMetabolism and Genetic Disorders

Cited by 284

The exogenous origin of trimethylamine in the mouse

Al-Waiz, M., Mikov, M., Mitchell, S. C., & Smith, R. L. (1992) · Metabolism

Gut microbiota and healthPolyamine Metabolism and Applications

Cited by 196

The fish odour syndrome: biochemical, familial, and clinical aspects.

Ayesh, R., Mitchell, S. C., Zhang, A., & Smith, R. L. (1993) · BMJ

Metabolism and Genetic DisordersSympathectomy and Hyperhidrosis Treatments

Cited by 160

Fish odour syndrome: Verification of carrier detection test

Zhang, A. Q., Mitchell, S., & Smith, R. (1995) · Journal of Inherited Metabolic Disease

Metabolism and Genetic DisordersAmino Acid Enzymes and Metabolism

Cited by 44

The relative importance of N-oxidation and N-demethylation in the metabolism of trimethylamine in man

Al-Waiz, M., Mitchell, S. C., Idle, J. R., & Smith, R. L. (1987) · Toxicology

Pharmacogenetics and Drug MetabolismPolyamine Metabolism and Applications

Cited by 34