A missense mutation at the [Gamma]42 secretase site in APP points to an essential role for N-truncated A[Beta]42 in Alzheimer's disease

Authors :: Van Broeckhoven, C.
Kumar-Singh, S.
De Jonghe, C.
Cruts, M.
Kleinert, R.
Wang, R.
Mercken, M. Vanderstichele, H.
Lofgren, A.
Vanmechelen, E.
Kroisel, P.M.
Source :: American Journal of Human Genetics. Oct, 2000, Vol. 67 Issue 4, 407
Publication Year :: 2000

Subjects :: Genetic research -- Analysis
Human genetics -- Research
Amyloid beta-protein -- Genetic aspects
Alzheimer's disease -- Genetic aspects
Biological sciences

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