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Liver Transplantation Prevents Progressive Neurological Impairment in Argininemia
Argininemia is a rare hereditary disease due to a deficiency of hepatic arginase, which is the last enzyme of the urea cycle and hydrolyzes arginine to ornithine and urea. The onset of the disease is usually in childhood, and clinical manifestations include progressive spastic paraparesis and mental...
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| Main Authors: | , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Springer Berlin Heidelberg
2013
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3755545/ https://ncbi.nlm.nih.gov/pubmed/23559324 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/8904_2013_218 |
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