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Identification of a novel germline SMARCB1 nonsense mutation in a family manifesting both schwannomatosis and unilateral vestibular schwannoma

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References

  1. Plotkin SR, Blakeley JO, Evans DG et al (2013) Update from the 2011 international schwannomatosis workshop: From genetics to diagnostic criteria. Am J Med Genet A 161A:405–416

    Article  PubMed  Google Scholar 

  2. Hulsebos TJ, Plomp AS, Wolterman RA, Robanus-Maandag EC, Baas F, Wesseling P (2007) Germline mutation of INI1/SMARCB1 in familial schwannomatosis. Am J Hum Genet 80:805–810

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  3. Piotrowski A, Xie J, Liu YF et al (2014) Germline loss-of-function mutations in LZTR1 predispose to an inherited disorder of multiple schwannomas. Nat Genet 46:182–187

    Article  PubMed Central  CAS  PubMed  Google Scholar 

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Correspondence to Qing Bi.

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Wu, J., Kong, M. & Bi, Q. Identification of a novel germline SMARCB1 nonsense mutation in a family manifesting both schwannomatosis and unilateral vestibular schwannoma. J Neurooncol 125, 439–441 (2015). https://doi.org/10.1007/s11060-015-1918-7

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  • DOI: https://doi.org/10.1007/s11060-015-1918-7

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