Journal Article

DKFZ-2017-02099

http://join2-wiki.gsi.de/foswiki/pub/Main/Artwork/join2_logo100x88.png Whole exome sequencing reveals that the majority of schwannomatosis cases remain unexplained after excluding SMARCB1 and LZTR1 germline variants.

Hutter, S. (First author)DKFZ* ; Piro, R. M.DKFZ* ; Reuss, D. E. ; Hovestadt, V.DKFZ* ; Sahm, F. ; Farschtschi, S. ; Kehrer-Sawatzki, H. ; Wolf, S.DKFZ* ; Lichter, P.DKFZ* ; von Deimling, A.DKFZ* ; Schuhmann, M. U.DKFZ* ; Pfister, S.DKFZ* ; Jones, D.DKFZ* ; Mautner, V. F.

2014
Springer Berlin

This record in other databases:

Please use a persistent id in citations: doi:10.1007/s00401-014-1311-1

Keyword(s): Chromosomal Proteins, Non-Histone ; DNA-Binding Proteins ; LZTFL1 protein, human ; SMARCB1 Protein ; SMARCB1 protein, human ; Transcription Factors

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Contributing Institute(s):

1. Pädiatrische Neuroonkologie (B062)
2. Molekulare Genetik (B060)
3. KKE Neuropathologie (G380)
4. DKTK Heidelberg (L101)
5. DKTK Tübingen (L801)

Research Program(s):

1. 312 - Functional and structural genomics (POF3-312) (POF3-312)

Appears in the scientific report 2014

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Database coverage:
; BIOSIS Previews ; Current Contents - Life Sciences ; Ebsco Academic Search ; IF >= 10 ; JCR ; NCBI Molecular Biology Database ; Nationallizenz ; SCOPUS ; Science Citation Index ; Science Citation Index Expanded ; Thomson Reuters Master Journal List ; Web of Science Core Collection

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