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Vitamin B6 in Primary Hyperoxaluria I: First Prospective Trial after 40 Years of Practice
BACKGROUND AND OBJECTIVES: Primary hyperoxaluria type I (PH I) is caused by deficiency of the liver-specific enzyme alanine-glyoxylate:aminotransferase (AGT). Many mutations are known to perturb AGT protein folding. Vitamin B6 (B6) is the only specific drug available for treatment. Although B6 has b...
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| Main Authors: | , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
American Society of Nephrology
2014
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3944765/ https://ncbi.nlm.nih.gov/pubmed/24385516 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2215/CJN.06820613 |
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