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Current and Future Treatments for Classic Galactosemia
Type I (classic) galactosemia, galactose 1-phosphate uridylyltransferase (GALT)-deficiency is a hereditary disorder of galactose metabolism. The current therapeutic standard of care, a galactose-restricted diet, is effective in treating neonatal complications but is inadequate in preventing burdenso...
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| 出版年: | J Pers Med |
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| 主要な著者: | , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
MDPI
2021
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7911353/ https://ncbi.nlm.nih.gov/pubmed/33525536 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/jpm11020075 |
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