Biochemistry and Genetics of gangliosidoses

Author:

Sandhoff K.,Christomanou Helene

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Reference287 articles.

1. Adachi, M., Schneck, L., Volk, B. W.: Progress in investigations of sphingolipidoses. Acta Neuropathol. (Berl.) 43, 1?18 (1978)

2. Andermann, E., Andermann, F., Carpenter, S., Karpati, G., Grimes, D., Wolfe, L. S.: Juvenile Tay-Sachs disease (late-onset GM2-gangliosidosis) in two Lebanese families. Clin. Res. 22, 738A (1974)

3. Andria, G., DelGiulice, C., Reuser, A. J. J.: Atypical expression of ?-galactosidase deficiency in a child with Hurler-like features but without neurological abnormalities. Clin. Genet. 14, 16?23 (1978)

4. Atsumi, T., Miyatake, T., Ohbuyashi, T., Mizuno, Y., Yoshida, M.: A case of Ramsey-Hunt syndrome with membranous cytoplasmatic bodies-like structures and ?-galactosidase deficiency. Proc. Annu. Meet. Jpn. Neurol. Soc. (1976)

5. Azzo, A. d', Hoogeveen, A., De Wit-Verbeek, H. A.: A rapid and simple microfractionation method for the analysis of hexosaminidase A and B activities in small numbers of cultured (amniotic fluid) cells. Clin. Chim. Acta 88, 1?7 (1978)

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