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Transport to cell surface of intestinal sucrase-isomaltase is blocked in the Golgi apparatus in a patient with congenital sucrase-isomaltase deficiency.

A case of congenital sucrase-isomaltase deficiency in man was investigated. An intestinal biopsy sample from a 5-year-old girl lacked sucrase but possessed low residual isomaltase activity. Immunoelectron microscopy with monoclonal antibodies to sucrase-isomaltase in biopsy samples from healthy subj...

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Détails bibliographiques
Publié dans:Proc Natl Acad Sci U S A
Auteurs principaux: Hauri, H P, Roth, J, Sterchi, E E, Lentze, M J
Format: Artigo
Langue:Inglês
Publié: National Academy of Sciences 1985
Sujets:
Accès en ligne:https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC391113/
https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/3925457/
https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.82.13.4423
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