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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Detalles Bibliográficos
Autores principales: Langen, H., von Kietzell, D., Byrd, D., Arslan-Kirchner, M., Vester, U., Stuhrmann, M., Dörk, T., Saar, K., Reis, A., Schmidtke, J., Brodehl, J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer-Verlag 2000
Materias:
Genetic Renal Disease / Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7102113/
https://www.ncbi.nlm.nih.gov/pubmed/10805464
http://dx.doi.org/10.1007/s004670050778

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7102113/
https://www.ncbi.nlm.nih.gov/pubmed/10805464
http://dx.doi.org/10.1007/s004670050778

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