Author:
Suzuki Yoshiyuki,Sakuraba Hitoshi,Potier Michel,Akagi Masao,Sakai Masao,Beppu Hirokuni
Publisher
Springer Science and Business Media LLC
Subject
Genetics(clinical),Genetics
Reference17 articles.
1. Galjaard H, D'Azzo A (1980) Relationship between clinical, biochemical and genetic heterogeneity in sialidase deficiency. International Symposium on sialidases and sialidoses, Genoa, Italy
2. Goldberg MF, Cotlier E, Fichenscher LG, Kenyon K, Enat R, Borowski SA (1971) Macular cherry-red spot, corneal clouding, and β-galactosidase deficiency: Clinical, biochemical, and electron microscopic study of a new autosomal recessive storage disease. Arch Intern Med 128:387–397
3. Hoogeveen AT, Verheijen FW, D'Azzo A, Galjaard H (1980) Genetic heterogeneity in human neuraminidase deficiency. Nature 285:500–502
4. Kobayashi T, Ohta M, Goto I, Tanaka Y, Kuroiwa Y (1979) Adult type mucolipidosis with β-galactosidase and sialidase deficiency. J Neurol 221:137–149
5. Kuriyama M, Okada S, Tanaka Y, Umezaki H (1980) Adult mucolipidosis with β-galactosidase and neuraminidase deficiencies. J Neurol Sci 46:245–254
Cited by
22 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