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Renal polyamine excretion, tubular amino acid reabsorption and molecular genetics in cystinuria
Cystinuria is an autosomal recessive disorder of the tubular and intestinal resorption of cystine, ornithine, lysine and arginine leading to nephrolithiasis. Three cystinuria types can be distinguished by the mode of inheritance (true recessive or intermediate) and by the pattern of the intestinal a...
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| Publicado no: | Pediatr Nephrol |
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| Main Authors: | , , , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Springer-Verlag
2000
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7102113/ https://ncbi.nlm.nih.gov/pubmed/10805464 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s004670050778 |
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