Schwannomatosis associated with multiple meningiomas due to a familial SMARCB1 mutation-Reference-Cited by-同舟云学术

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Schwannomatosis associated with multiple meningiomas due to a familial SMARCB1 mutation

Published:2009-07-07 Issue:1 Volume:11 Page:73-80
ISSN:1364-6745
Container-title:neurogenetics
language:en
Short-container-title:Neurogenetics

Author:

Bacci Costanza,Sestini Roberta,Provenzano Aldesia,Paganini Irene,Mancini Irene,Porfirio Berardino,Vivarelli Rossella,Genuardi Maurizio,Papi Laura

Publisher

Springer Science and Business Media LLC

Subject

Cellular and Molecular Neuroscience,Genetics (clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1007/s10048-009-0204-2.pdf

Reference36 articles.

1. Huang JH, Simon SL, Nagpal S, Nelson PT, Zager EL (2004) Management of patients with schwannomatosis: report of six cases and review of the literature. Surg Neurol 62:353–361. doi: 10.1016/j.surneu.2003.11.020

2. Jacoby LB, Jones D, Davis K, Kronn D, Short MP, Gusella J, MacCollin M (1997) Molecular analysis of the NF2 tumor-suppressor gene in schwannomatosis. Am J Hum Genet 61:1293–1302. doi: 10.1086/301633

3. 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. doi: 10.1086/513207

4. Boyd C, Smith MJ, Kluwe L, Balogh A, Maccollin M, Plotkin SR (2008) Alterations in the SMARCB1 (INI1) tumor suppressor gene in familial schwannomatosis. Clin Genet 74:358–366. doi: 10.1111/j.1399-0004.2008.01060.x

5. Hadfield KD, Newman WG, Bowers NL, Wallace A, Bolger C, Colley A, McCann E, Trump D, Prescott T, Evans DG (2008) Molecular characterisation of SMARCB1 and NF2 in familial and sporadic schwannomatosis. J Med Genet 45:332–339. doi: 10.1136/jmg.2007.056499

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