Loss of SOX10 function contributes to the phenotype of human Merlin-null schwannoma cells.
Doddrell RD; Dun XP; Shivane A; Feltri ML; Wrabetz L; Wegner M; Sock E; Hanemann CO; Parkinson DB; Brain: A Journal Of Neurology, 2013, vol. 136, issue Pt 2, p 549, ISSN 14602156. ISBN 14602156.

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