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Progress toward cell-directed therapy for phenylketonuria

Phenylketonuria (PKU) is one of the most common inborn errors of metabolism with an annual incidence of approximately 1:16,000 live births in North America. Contemporary therapy relies upon lifelong dietary protein restriction and supplementation with phenylalanine-free medical foods. This therapy i...

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Detalhes bibliográficos
Autor principal: Harding, CO
Formato: Artigo
Idioma:Inglês
Publicado em: 2008
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2694058/
https://ncbi.nlm.nih.gov/pubmed/18498375
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/j.1399-0004.2008.01027.x
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