LIS1 and XLIS ( DCX ) mutations cause most classical lissencephaly, but different patterns of malformation.
Pilz, Daniela T.; Matsumoto, Naomichi; Minnerath, Sharon; Mills, Patti; Gleeson, Joseph G.; Allen, Kristin M.; Walsh, Christopher A.; Barkovich, A. James; Dobyns, William B.; Ledbetter, David H.; Ross, M. Elizabeth; Human Molecular Genetics, 1998, vol. 7, issue 13, ISSN 09646906. ISBN 09646906.

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