杜氏型肌营养不良患儿及基因携带者的血清α-半乳糖苷酶活性
Serum alpha-galactosidase activity in children with Duchenne-type muscular dystrophy and in gene carriers.
作者信息
László A, Havass Z
出版信息
Acta Paediatr Hung. 1983;24(4):327-9.
PMID:6324830
Abstract
Serum alpha-galactosidase activity was studied in 21 control children, 15 children with Duchenne muscular dystrophy, and in 8 gene carrier mothers. In both the DMD hemi- and the heterozygous groups a significant increase of alpha-galactosidase activity was demonstrated.
摘要
对21名对照儿童、15名杜氏肌营养不良症儿童以及8名基因携带者母亲的血清α-半乳糖苷酶活性进行了研究。在杜氏肌营养不良症半合子组和杂合子组中，均显示出α-半乳糖苷酶活性显著增加。
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Serum alpha-galactosidase activity in children with Duchenne-type muscular dystrophy and in gene carriers.杜氏型肌营养不良患儿及基因携带者的血清α-半乳糖苷酶活性
Acta Paediatr Hung. 1983;24(4):327-9.
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