Germline loss-of-function mutations in LZTR1 predispose to an inherited disorder of multiple schwannomas
Nature Genetics2013Vol. 46(2), pp. 182–187
Citations Over TimeTop 1% of 2013 papers
Arkadiusz Piotrowski, Jing Xie, Ying F Liu, Andrzej Poplawski, Alicia Gomes, Piotr Madanecki, Chuanhua Fu, Michael R. Crowley, David K. Crossman, Linlea Armstrong, Dusica Babovic‐Vuksanovic, Amanda L. Bergner, Jaishri O. Blakeley, Andrea Blumenthal, Molly S. Daniels, Howard Feit, Kathy Gardner, Stephanie Hurst, Christine Kobelka, Chung Lee, Rebecca Nagy, Katherine A. Rauen, John M. Slopis, Pim Suwannarat, Judith A. Westman, Andrea Zanko, Bruce R. Korf, Ludwine Messiaen
Related Papers
- → Targeted next-generation sequencing for differential diagnosis of neurofibromatosis type 2, schwannomatosis, and meningiomatosis(2018)66 cited
- → Deep intronic hotspot variant explaining rhabdoid tumor predisposition syndrome in two patients with atypical teratoid and rhabdoid tumor(2017)9 cited
- Loss of NF2 Gene in Neurofibromatosis Type 2－ Associated Cutaneous Schwannomas(2001)
- → ATRT-11. PREVALENCE OF GERMLINE VARIANTS IN SMARCB1 INCLUDING SOMATIC MOSAICISM IN AT/RT AND OTHER RHABDOID TUMORS(2020)
- → The Molecular Genetics of Schwannomatosis(2009)