https://t.co/nHZ7hG9eWe Oct 2017 The complete European guidelines on phenylketonuria: diagnosis & treatment Phenylketonuria (PKU) is autosomal recessive inborn error of phenylalanine metabolism caused by deficiency in enzyme phenylalanine hydroxylase
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Dr. Öğr. Üyesi Burcu Hişmi ile fenilketonüri diyet tedavisi uygulamaları üzerine konuşuyoruz. Moderatör: Dr. Ayşe Kılıç İlgili makale linki: https://t.co/wi7C92T2E8 https://t.co/eRSrYDx8dA Instagram: metacademymetabolism [email protected]">@gmail.com">[email protected] http
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Um bom ponto de partida para quem tenha interesse em perceber a ciência por trás da fenilcetonúria. The complete European guidelines on phenylketonuria: diagnosis and treatment (2017) https://t.co/JJuFpKVbYC
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RT @Biblioteca_SJD: The complete European guidelines on phenylketonuria: diagnosis and treatment https://t.co/1U5SihkgGl #PublicaSJDBarcelona @SJDbarcelona_es