Clinical utility gene card for: Trimethylaminuria - update 2014

Eur J Hum Genet. 2015 Sep;23(9). doi: 10.1038/ejhg.2014.226. Epub 2014 Oct 22.

Authors

Elizabeth A Shephard¹, Eileen P Treacy², Ian R Phillips³

Affiliations

¹ Institute of Structural and Molecular Biology, University College London, London, UK.
² 1] National Centre for Inherited Metabolic Disorders, Children's University Hospital, Dublin, Ireland [2] Trinity College, Dublin, Ireland.
³ 1] Institute of Structural and Molecular Biology, University College London, London, UK [2] School of Biological and Chemical Sciences, Queen Mary University of London, London, UK.

No abstract available

MeSH terms

Diet
Disease Management
Female
Gene Expression
Humans
Incidence
Male
Metabolism, Inborn Errors / diagnosis*
Metabolism, Inborn Errors / epidemiology
Metabolism, Inborn Errors / genetics*
Metabolism, Inborn Errors / pathology
Methylamines / urine*
Mutation*
Oxygenases / genetics*
Sex Factors
United Kingdom / epidemiology

Substances

Methylamines
Oxygenases
dimethylaniline monooxygenase (N-oxide forming)

Supplementary concepts

Trimethylaminuria

Grants and funding

MR/K015494/1/MRC_/Medical Research Council/United Kingdom