Loss of SOX10 function contributes to the phenotype of human Merlin-null schwannoma cells.
Doddrell, Robin D. S.; Dun, Xin-Peng; Shivane, Aditya; Feltri, M. Laura; Wrabetz, Lawrence; Wegner, Michael; Sock, Elisabeth; Hanemann, C. Oliver; Parkinson, David B.; Brain: A Journal of Neurology, 2013, vol. 136, issue 2, p 549, ISSN 00068950. ISBN 14602156.

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