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Transient Massive Trimethylaminuria Associated with Food Protein–Induced Enterocolitis Syndrome

Trimethylaminuria (TMAU) is an autosomal recessive disease caused by excessive excretion into body fluids and breath of unoxidized trimethylamine (TMA) derived from the enterobacterial metabolism of dietary precursors. The condition is caused by deficiency of flavin-containing monooxygenase 3 (FMO3)...

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Detaylı Bibliyografya
Asıl Yazarlar: Miller, Natalie B., Beigelman, Avraham, Utterson, Elizabeth, Shinawi, Marwan
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Springer International Publishing 2013
Konular:
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC3897788/
https://ncbi.nlm.nih.gov/pubmed/23821320
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/8904_2013_238
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