The characteristics of acid 1,4-alpha-glucosidase in various human adult and fetal tissues.
作者信息
Shin-Bühring Y S, Unterreithmeier J, Wilsmann T, Schaub J
出版信息
J Inherit Metab Dis. 1978;1(4):159-60. doi: 10.1007/BF01805586.
PMID:41975
Abstract
摘要
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本文引用的文献
1
alpha-Glucosidase deficiency in generalized glycogenstorage disease (Pompe's disease).全身性糖原贮积病（庞贝氏病）中的α-葡萄糖苷酶缺乏症。
Biochem J. 1963 Jan;86(1):11-6. doi: 10.1042/bj0860011.
2
Tissue alpha-glucosidase activity and glycogen content in patients with generalized glycogenosis.
Isr J Med Sci. 1967 May-Jun;3(3):411-21.
3
Deficiency of acid alpha glucosidase in the urine of patients with Pompe's disease.庞贝病患者尿液中酸性α-葡萄糖苷酶缺乏。
J Pediatr. 1973 Feb;82(2):294-7. doi: 10.1016/s0022-3476(73)80174-x.
4
Separation of acid and neutral alpha-glucosidase isoenzymes from fetal and adult tissues, cultivated fibroblasts and amniotic fluid cells by DEAE-cellulose and sephadex G-100 column chromatography.通过DEAE-纤维素和葡聚糖凝胶G-100柱色谱法从胎儿和成人组织、培养的成纤维细胞及羊水细胞中分离酸性和中性α-葡萄糖苷酶同工酶。
Clin Chim Acta. 1978 Nov 1;89(3):393-404. doi: 10.1016/0009-8981(78)90401-1.
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