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...

Descripción completa

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

Internet

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

Ejemplares similares