Disruption of murine Hexa gene leads to enzymatic deficiency and to neuronal lysosomal storage, similar to that observed in Tay-Sachs disease-Reference-Cited by-同舟云学术

Disruption of murine Hexa gene leads to enzymatic deficiency and to neuronal lysosomal storage, similar to that observed in Tay-Sachs disease

Published:1995-12 Issue:12 Volume:6 Page:844-849
ISSN:0938-8990
Container-title:Mammalian Genome
language:en
Short-container-title:Mammalian Genome

Author:

Cohen-Tannoudji M.,Marchand P.,Akli S.,Sheardown S. A.,Puech J. P.,Kress C.,Gressens P.,Nassogne M. C.,Beccari T.,Muggleton-Harris A. L.,Evrard P.,Stirling J. L.,Poenaru L.,Babinet C.

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://link.springer.com/content/pdf/10.1007/BF00292433.pdf

Reference38 articles.

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2. Akli, S., Chelly, J., Lacorte, J.M., Poenaru, L., Kahn, A. (1991). Seven novel Tay-Sachs mutations detected by chemical mismatch cleavage of PCR-amplified cDNA fragments. Genomics 11, 124?134.

3. Akli, S., Boué, J., Kleijer, W., Vamos, E., Young, E., Gatti, R., DiNatale, P., Motte, A., Vanier, M.T., Maire, I., Miranda, C., Salvaire, R., Sandhoff, K., Poenaru, L. (1993). Collaborative study of molecular epidemiology of Tay-Sachs disease in Europe. Eur. J. Hum. Genet. 1, 229?238.

4. Andermann, E., Andermann, F., Patry, G., Lafontaine, R., Geoffroy, G., Seriver, C.R., Wolfe, L.S. (1971). Tay-Sachs disease in Quebec: evidence for a geographic aggregate in the French-Canadian population with identification of a new retardation syndrome with possible linkage to the Tay-Sachs gene. Trans. Am. Neurol. Assoc. 98, 17?21.

5. Bapat, B., Ethier, M., Neote, K., Mahuran, D., Gravel, R.A. (1988). Cloning and sequence of a cDNA encoding the ?-subunit of mouse ?-hexosaminidase. FEBS Lett. 237, 191?195.

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