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592 Clinical follow up of Swedish families with APP and presenilin I mutations
L.O. Wahlund, H. Basun, O. Ahnkvist, P. Julin, M. Viitanen, K. Axelman, A. Nordberg, M. Shigeta, V. Jelic, L. LannfeltVolume:
17
Year:
1996
Language:
english
DOI:
10.1016/s0197-4580(96)80594-x
File:
PDF, 142 KB
english, 1996