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Primary structure and processing of lysosomal alpha-glucosidase; homology with the intestinal sucrase-isomaltase complex.

Lysosomal alpha-glucosidase (acid maltase) is essential for degradation of glycogen in lysosomes. Enzyme deficiency results in glycogenosis type II. The amino acid sequence of the entire enzyme was derived from the nucleotide sequence of cloned cDNA. The cDNA comprises 3636 nt, and hybridizes with a...

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Detalhes bibliográficos
Main Authors: Hoefsloot, L H, Hoogeveen-Westerveld, M, Kroos, M A, van Beeumen, J, Reuser, A J, Oostra, B A
Formato: Artigo
Idioma:Inglês
Publicado em: 1988
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC457155/
https://ncbi.nlm.nih.gov/pubmed/3049072
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