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Article

Whole exome sequencing reveals that the majority of schwannomatosis cases remain unexplained after excluding SMARCB1 and LZTR1 germline variants.

Acta neuropathologica - 1 Sept 2014

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

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Share to Chromosomal Proteins, Non-Histone
Share to Chromosomes, Human, Pair 22
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 25008767
DOI: 10.1007/s00401-014-1311-1

Genes

LZTR1
SMARCB1

Provenance

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Whole exome sequencing reveals that the majority of schwannomatosis cases remain unexplained after excluding SMARCB1 and LZTR1 germline variants.PMID 25008767Read ↗

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