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Intestinal absorption in lysinuric protein intolerance: impaired for diamino acids, normal for citrulline.
Lysinuric protein intolerance (LPI) is an autosomal recessive defect of diamino acid transport characterised by massive diaminoaciduria, especially lysinuria, with hyperammonaemia after heavy nitrogen intake. The defect has previously been demonstrated in the kidney, and is probably present in the l...
Tallennettuna:
Päätekijät: | , , |
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Aineistotyyppi: | Artigo |
Kieli: | Inglês |
Julkaistu: |
1980
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Aiheet: | |
Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1419667/ https://ncbi.nlm.nih.gov/pubmed/6776014 |
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