Whole exome sequencing reveals that the majority of schwannomatosis cases remain unexplained after excluding SMARCB1 and LZTR1 germline variants
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Abstract
Bibliographical data
Original language | English |
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ISSN | 0001-6322 |
DOIs | |
Publication status | Published - 01.09.2014 |
PubMed | 25008767 |
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