Clinicopathological features of familial Alzheimer's disease associated with the M139V mutation in the presenilin 1 gene. Pedigree but not mutation specific age at onset provides evidence for a further genetic factor.
| Autor: | Fox, N C, Kennedy, A M, Harvey, R J, Lantos, P L, Roques, P K, Collinge, J, Hardy, J, Hutton, M, Stevens, J M, Warrington, E K, Rossor, M N |
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| Zdroj: | Brain: A Journal of Neurology; 1997, Vol. 120 Issue 3, p491-501, 11p |
| Databáze: | Complementary Index |
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