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• W2157244035 abstract "American Journal of Medical Genetics Part AVolume 152A, Issue 6 p. 1586-1587 Research Letter Isolated unilateral vestibular schwannomas do not harbor HRAS mutations†‡ Miriam J. Smith, Miriam J. Smith Department of Medical Genetics, St Mary's Hospital, Manchester Academic Health Sciences Centre (MAHSC), University of Manchester, Manchester, UKSearch for more papers by this authorKristen D. Hadfield, Kristen D. Hadfield Department of Medical Genetics, St Mary's Hospital, Manchester Academic Health Sciences Centre (MAHSC), University of Manchester, Manchester, UKSearch for more papers by this authorRichard T. Ramsden, Richard T. Ramsden Department of Neurosurgery, Hope Hospital, Salford, Manchester, UKSearch for more papers by this authorScott A. Rutherford, Scott A. Rutherford Department of Neurosurgery, Hope Hospital, Salford, Manchester, UKSearch for more papers by this authorAndrew T. King, Andrew T. King Department of Neurosurgery, Hope Hospital, Salford, Manchester, UKSearch for more papers by this authorWilliam G. Newman, William G. Newman Department of Medical Genetics, St Mary's Hospital, Manchester Academic Health Sciences Centre (MAHSC), University of Manchester, Manchester, UKSearch for more papers by this authorD. Gareth Evans, Corresponding Author D. Gareth Evans [email protected] Department of Medical Genetics, St Mary's Hospital, Manchester Academic Health Sciences Centre (MAHSC), University of Manchester, Manchester, UKDepartment of Genetic Medicine, Manchester Academic Health Sciences Centre (MAHSC), St Mary's Hospital, University of Manchester, Manchester M13 9WL, UK.Search for more papers by this author Miriam J. Smith, Miriam J. Smith Department of Medical Genetics, St Mary's Hospital, Manchester Academic Health Sciences Centre (MAHSC), University of Manchester, Manchester, UKSearch for more papers by this authorKristen D. Hadfield, Kristen D. Hadfield Department of Medical Genetics, St Mary's Hospital, Manchester Academic Health Sciences Centre (MAHSC), University of Manchester, Manchester, UKSearch for more papers by this authorRichard T. Ramsden, Richard T. Ramsden Department of Neurosurgery, Hope Hospital, Salford, Manchester, UKSearch for more papers by this authorScott A. Rutherford, Scott A. Rutherford Department of Neurosurgery, Hope Hospital, Salford, Manchester, UKSearch for more papers by this authorAndrew T. King, Andrew T. King Department of Neurosurgery, Hope Hospital, Salford, Manchester, UKSearch for more papers by this authorWilliam G. Newman, William G. Newman Department of Medical Genetics, St Mary's Hospital, Manchester Academic Health Sciences Centre (MAHSC), University of Manchester, Manchester, UKSearch for more papers by this authorD. Gareth Evans, Corresponding Author D. Gareth Evans [email protected] Department of Medical Genetics, St Mary's Hospital, Manchester Academic Health Sciences Centre (MAHSC), University of Manchester, Manchester, UKDepartment of Genetic Medicine, Manchester Academic Health Sciences Centre (MAHSC), St Mary's Hospital, University of Manchester, Manchester M13 9WL, UK.Search for more papers by this author First published: 14 May 2010 https://doi.org/10.1002/ajmg.a.33409 † Approval for the study was provided by the local ethics committee. Informed consent was obtained from patients and their families for publication of their data in this report. ‡ How to cite this article: Smith MJ, Hadfield KD, Ramsden RT, Rutherford SA, King AT, Newman WG, Evans DG. 2010. Isolated unilateral vestibular schwannomas do not harbor HRAS mutations. Am J Med Genet Part A 152A:1586–1587. Read the full textAboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Share a linkShare onEmailFacebookTwitterLinkedInRedditWechat No abstract is available for this article. REFERENCES Ahronowitz I, Xin W, Kiely R, Sims K, MacCollin M, Nunes FP. 2007. Mutational spectrum of the NF2 gene: A meta-analysis of 12 years of research and diagnostic laboratory findings. Hum Mutat 28: 1–12. Aoki Y, Niihori T, Kawame H, Kurosawa K, Ohashi H, Tanaka Y, Filocamo M, Kato K, Suzuki Y, Kure S, Matsubara Y. 2005. Germline mutations in HRAS proto-oncogene cause Costello syndrome. Nat Genet 37: 1038–1040. Baser ME. 2006. The distribution of constitutional and somatic mutations in the neurofibromatosis 2 gene. Hum Mutat 27: 297–306. Czeizel AE, Timar L. 1995. Hungarian case with Costello syndrome and translocation t(1,22). Am J Med Genet 57: 501–503. Flotho C, Steinemann D, Mullighan CG, Neale G, Mayer K, Kratz CP, Schlegelberger B, Downing JR, Niemeyer CM. 2007. Genome-wide single-nucleotide polymorphism analysis in juvenile myelomonocytic leukemia identifies uniparental disomy surrounding the NF1 locus in cases associated with neurofibromatosis but not in cases with mutant RAS or PTPN11. Oncogene 26: 5816–5821. Gripp KW. 2005. Tumor predisposition in Costello syndrome. Am J Med Genet Part C 137C: 72–77. Jung JR, Kim H, Jeun SS, Lee JY, Koh EJ, Ji C. 2005. The Phosphorylation status of merlin is important for regulating the Ras-ERK pathway. Mol Cells 20: 196–200. Kim HA, Rosenbaum T, Marchionni MA, Ratner N, DeClue JE. 1995. Schwann cells from neurofibromin deficient mice exhibit activation of p21ras, inhibition of cell proliferation and morphological changes. Oncogene 11: 325–335. Neurofibromatosis Conference Statement. 1988. Neurofibromatosis. Conference statement. National Institutes of Health Consensus Development Conference. Arch Neurol 45:575–578. Suri M, Garrett C. 1998. Costello syndrome with acoustic neuroma and cataract. Is the Costello locus linked to neurofibromatosis type 2 on 22q? Clin Dysmorphol 7: 149–151. Sutajova M, Neukirchen U, Meinecke P, Czeizel AE, Tımar L, Solyom E, Gal A, Kutschea K. 2003. Disruption of the PDGFB gene in a 1;22 translocation patient does not cause Costello syndrome. Genomics 83: 883–892. Welling DB. 1998. Clinical manifestations of mutations in the neurofibromatosis type 2 gene in vestibular schwannomas (acoustic neuromas). Laryngoscope 108: 178–189. Volume152A, Issue6June 2010Pages 1586-1587 ReferencesRelatedInformation" @default.
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