Familial Alzheimer's disease: Site of mutation influences clinical phenotype.
Autor: | Lippa, C. F., Swearer, J. M., Kane, K. J., Nochlin, D., Bird, T. D., Ghetti, B., Nee, L. E., St. George-Hyslop, P., Pollen, D. A., Drachman, D. A. |
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Zdroj: | Annals of Neurology; 2000, Vol. 48 Issue 3, p376-379, 4p |
Databáze: | Complementary Index |
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