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Drosophila melanogaster models of galactosemia
The galactosemias are a family of autosomal recessive genetic disorders resulting from impaired function of the Leloir Pathway of galactose metabolism. Type I, or classic galactosemia, results from profound deficiency of galactose-1-phosphate uridylyltransferase (GALT), the second enzyme in the Lelo...
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| Publicado en: | Curr Top Dev Biol |
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| Main Authors: | , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
2016
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5683716/ https://ncbi.nlm.nih.gov/pubmed/28057307 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/bs.ctdb.2016.07.009 |
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