[Glycogenosis type II; acid alpha-glucosidase deficiency]

Autor: T, Hirayasu, K, Chinen, H, Sakuda, T, Iwamasa
Rok vydání: 1995
Předmět:
Zdroj: Nihon rinsho. Japanese journal of clinical medicine. 53(12)
ISSN: 0047-1852
Popis: Knowledge of the general enzymology of lysosomal acid alpha-glucosidase (acid maltase) including that of the intracellular processing mechanism and of the cDNA sequence has advanced recently. Genetic heterogeneity of the mRNA of acid alpha-glucosidase deficient patients has also been reported. Referring to these recent advances, and based on our previously reported results, the pathologic aspects of the disease are reviewed. Heterogeneity of the enzyme molecules themselves and their characteristics in various tissues are also demonstrated.
Databáze: OpenAIRE