Author:
Aula P.,Raivio K. O.,Maury P.
Subject
Genetics(clinical),Genetics
Reference16 articles.
1. Aula, P., NÄntö, V., Laipio, M-L. and Autio, S. Aspartylglucosaminuria: deficiency of aspartylglucosaminidase in cultured fibroblasts of patients and their heterozygous parents.Clin. Genet. 4 (1973) 297
2. Aula, P., Raivio, K. O. and Autio, S. Enzymatic diagnosis and carrier detection of aspartylglucosaminuria using blood samples.Pediatr. Res. 10 (1976) 625
3. Autio, S. Aspartylglucosaminuria. Analysis of 34 patients.J. Ment. Defic. Res., Monogr. Ser. 1 (1972) 1
4. Borud, O., Strömme, J. H., Lie, S. O. and Torp, K. H. Aspartylglucosaminuria in northern Norway in eight patients: clinical heterogeneity and variations with the diet.J. Inher. Metab. Dis. 1 (1978) 95
5. Hakomori, S. I. A rapid permethylation of glycolipid and polysaccharide catalyzed by methylsulfinyl carbanion in dimethyl sulfoxide.J. Biochem. (Tokyo) 55 (1964) 205
Cited by
8 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献