Newborn screening for inborn errors of metabolism

Currently in Norway, we screen our newborn for two inherited metabolic disorders: Congenital hypothyroidism (CH) and Phenylketonuria (PKU). There is now a proposal to expand the newborn screening program with an additional 19 inherited metabolic disorders: 1. Maple syrup urine disease, MSUD 2. Tyros...

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Detalles Bibliográficos
Otros Autores: Vist, Gunn E., author (author)
Formato: Libro electrónico
Idioma:Inglés
Publicado: Oslo, Norway : Norwegian Knowledge Centre for the Health Services 2007.
Materias:
Ver en Biblioteca Universitat Ramon Llull:https://discovery.url.edu/permalink/34CSUC_URL/1im36ta/alma991009816706506719

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