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Fish odor syndrome (trimethylaminuria) supporting the possible FMO3 down expression in childhood: a case report

INTRODUCTION: Trimethylaminuria is a rare inherited disorder due to decreased metabolism of dietary-derived trimethylamine by flavin-containing monooxygenase 3. Several single nucleotide polymorphisms of the flavin-containing monooxygenase 3 gene have been described and result in an enzyme with decr...

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Detalles Bibliográficos
Autores principales:	D’Angelo, Rosalia, Scimone, Concetta, Esposito, Teresa, Bruschetta, Daniele, Rinaldi, Carmela, Ruggeri, Alessia, Sidoti, Antonina
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	BioMed Central 2014
Materias:	Case Report
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4190592/ https://www.ncbi.nlm.nih.gov/pubmed/25288227 http://dx.doi.org/10.1186/1752-1947-8-328

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