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Alkaptonuric ochronosis: Report of a case and brief review
Alkaptonuria, a metabolic disorder characterized by a triad of homogentisic aciduria, arthritis and ochronosis is one of the first conditions in the charter of group of inborn errors of metabolism proposed to have Mendelian recessive inheritance. It is due to the deficiency of the enzyme homogentisi...
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| Main Authors: | , , |
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| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
Springer India
2007
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| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3453790/ https://ncbi.nlm.nih.gov/pubmed/23105706 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/BF02913337 |
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