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Analysis of six novel flavin-containing monooxygenase 3 (FMO3) gene variants found in a Japanese population suffering from trimethylaminuria

Polymorphic human flavin-containing monooxygenase 3 (FMO3) is associated with the inherited disorder trimethylaminuria. Several FMO3 variants have been observed in a variety of ethnic groups, including a Japanese cohort suffering from trimethylaminuria. The aim of this study was to screen another se...

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Dades bibliogràfiques
Publicat a:Mol Genet Metab Rep
Autors principals: Shimizu, Makiko, Origuchi, Yumi, Ikuma, Marika, Mitsuhashi, Nanako, Yamazaki, Hiroshi
Format: Artigo
Idioma:Inglês
Publicat: Elsevier 2015
Matèries:
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC5471399/
https://ncbi.nlm.nih.gov/pubmed/28649550
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ymgmr.2015.10.013
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