Whole exome sequencing reveals that the majority of schwannomatosis cases remain unexplained after excluding SMARCB1 and LZTR1 germline variants.
作者信息
Hutter Sonja, Piro Rosario M, Reuss David E, Hovestadt Volker, Sahm Felix, Farschtschi Said, Kehrer-Sawatzki Hildegard, Wolf Stephan, Lichter Peter, von Deimling Andreas, Schuhmann Martin U, Pfister Stefan M, Jones David T W, Mautner Victor F
机构信息
Division of Pediatric Neurooncology, German Cancer Research Center (DKFZ), Im Neuenheimer Feld 280, 69120, Heidelberg, Germany.
出版信息
Acta Neuropathol. 2014 Sep;128(3):449-52. doi: 10.1007/s00401-014-1311-1. Epub 2014 Jul 10.
PMID:25008767
Abstract
摘要
Zotero 插件