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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Bibliografski detalji
Glavni autori: D’Angelo, Rosalia, Scimone, Concetta, Esposito, Teresa, Bruschetta, Daniele, Rinaldi, Carmela, Ruggeri, Alessia, Sidoti, Antonina
Format: Artigo
Jezik:Inglês
Izdano: BioMed Central 2014
Teme:
Case Report
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC4190592/
https://ncbi.nlm.nih.gov/pubmed/25288227
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1752-1947-8-328
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