Ballabio A, Pallini R, Di Natale P
Clin Genet. 1984 Feb;25(2):191-5. doi: 10.1111/j.1399-0004.1984.tb00484.x.
Cell fusion with polyethylene glycol (PEG) was performed on fibroblasts from a previously studied patient with a mild form of Sanfilippo B disease and altered residual enzyme activity and fibroblasts from several patients with the classical, severe form of the disease. No complementation was found in heterokaryons. This suggests that the mild phenotype in our patient can be ascribed to an allelic mutation.
使用聚乙二醇(PEG)对一名先前研究过的患有轻度桑菲利波B病且残余酶活性改变的患者的成纤维细胞,以及几名患有典型重度该病的患者的成纤维细胞进行细胞融合。在异核体中未发现互补现象。这表明我们患者的轻度表型可归因于等位基因突变。