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Galactosemia: Towards Pharmacological Chaperones

Galactosemia is a rare inherited metabolic disease resulting from mutations in the four genes which encode enzymes involved in the metabolism of galactose. The current therapy, the removal of galactose from the diet, is inadequate. Consequently, many patients suffer lifelong physical and cognitive d...

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Detalhes bibliográficos
Publicado no:J Pers Med
Main Authors: Banford, Samantha, McCorvie, Thomas J., Pey, Angel L., Timson, David J.
Formato: Artigo
Idioma:Inglês
Publicado em: MDPI 2021
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7914515/
https://ncbi.nlm.nih.gov/pubmed/33562227
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/jpm11020106
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