G476(P) Trimethylaminuria: A case report | Archives of Disease in Childhood

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British Inherited Metabolic Disease Group: British Society for Paediatric Endocrinology and Diabetes

G476(P) Trimethylaminuria: A case report

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Cite this article as:: Sabir N, Padmakumar B

G476(P) Trimethylaminuria: A case report

Archives of Disease in Childhood 2014;99:A197.