Combination of variant P.PRO153LEU and P.GLU158LYS polymorphism in FMO3 gene cause of “MILD” fish odor syndrome in a child of 2 years

Álvarez, S. Izquierdo; Valle, A. RodrÍguez; Gallart, M.D. Miramar; Villarroya, M.J. Alcaine; Pueyo, C. Lahuerta; LÓpez, J.J. Ochoa; Hevia, J.I. GonzÁlez; JimÉnez, I. GarcÍa; Puente, J.

doi:10.1016/j.cca.2019.03.477

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Combination of variant P.PRO153LEU and P.GLU158LYS polymorphism in FMO3 gene cause of “MILD” fish odor syndrome in a child of 2 years

Author(s): S. Izquierdo Álvarez , A. RodrÍguez Valle , M.D. Miramar Gallart , M.J. Alcaine Villarroya , C. Lahuerta Pueyo , J.J. Ochoa LÓpez , J.I. GonzÁlez Hevia , I. GarcÍa JimÉnez , J. Puente

Publication date Created: June 2019

Publication date (Print): June 2019

Journal: Clinica Chimica Acta

Publisher: Elsevier BV

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Title: Clinica Chimica Acta

Abbreviated Title: Clinica Chimica Acta

Publisher: Elsevier BV

ISSN (Print): 00098981

Publication date Created: June 2019

Publication date (Print): June 2019

Volume: 493

Pages: S230-S231

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DOI: 10.1016/j.cca.2019.03.477

SO-VID: 96acef24-0e1a-477c-8d59-70022f562ab9

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Combination of variant P.PRO153LEU and P.GLU158LYS polymorphism in FMO3 gene cause of “MILD” fish odor syndrome in a child of 2 years

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