Cortical dysplasia resembling human type 2 lissencephaly in mice lacking all three APP family members.
Herms J; Anliker B; Heber S; Ring S; Fuhrmann M; Kretzschmar H; Sisodia S; Müller U; The EMBO Journal, 2004, vol. 23, issue 20, p 4106, ISSN 02614189. ISBN 02614189.

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