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Proepper, Christiane R. , Schwarz, Lisa-Maria, Schuetz, Sofia M., von Au, Katja, Bast, Thomas, Beaud, Nathalie, Borggraefe, Ingo, Bosch, Friedrich, Busse, Melanie, Chung, Jena, Debus, Otfried, Diepold, Katharina, Fries, Thomas, von Gersdorff, Gero, Haeussler, Martin, Hahn, Andreas, Hartlieb, Till, Heiming, Ralf, Herkenrath, Peter, Kluger, Gerhard, Kreth, Jonas H., Kurlemann, Gerhard, Moeller, Peter, Morris-Rosendahl, Deborah J. , Panzer, Axel, Philippi, Heike, Ruegner, Sophia, Toepfer, Carolina, Vieker, Silvia, Wiemer-Kruel, Adelheid, Winter, Anika, Schuierer, Gerhard, Hehr, Ute und Geis, Tobias (2026) Gene-specific long-term course, neurodevelopmental outcome and quality of life in patients with LIS1/PAFAH1B1-, DCX-, DYNC1H1-, TUBA1A- and TUBG1-related lissencephaly. Orphanet Journal of Rare Diseases 21, S. 206.