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Congenital sucrase-isomaltase deficiency arising from cleavage and secretion of a mutant form of the enzyme

Congenital sucrase-isomaltase deficiency (CSID) is an autosomal recessive human intestinal disorder that is clinically characterized by fermentative diarrhea, abdominal pain, and cramps upon ingestion of sugar. The symptoms are the consequence of absent or drastically reduced enzymatic activities of...

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Главные авторы: Jacob, Ralf, Zimmer, Klaus-Peter, Schmitz, Jacques, Naim, Hassan Y.
Формат: Artigo
Язык:Inglês
Опубликовано: American Society for Clinical Investigation 2000
Предметы:
Online-ссылка:https://ncbi.nlm.nih.gov/pmc/articles/PMC314311/
https://ncbi.nlm.nih.gov/pubmed/10903344
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