Whole exome sequencing reveals that the majority of schwannomatosis cases remain unexplained after excluding SMARCB1 and LZTR1 germline variants
Sonja Hutter,Rosario M. Piro,David E. Reuss,Volker Hovestadt…Volume:
128
Language:
english
Journal:
Acta Neuropathologica
DOI:
10.1007/s00401-014-1311-1
Date:
September, 2014
File:
PDF, 603 KB
english, 2014