Cortical dysplasia resembling human type 2 lissencephaly in mice lacking all three APP family members.

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Published in EMBO J on September 23, 2004

Authors

Jochen Herms1, Brigitte Anliker, Sabine Heber, Sabine Ring, Martin Fuhrmann, Hans Kretzschmar, Sangram Sisodia, Ulrike Müller

Author Affiliations

1: Zentrum für Neuropathologie und Prionforschung, Universität München, München, Germany.

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