C. Lu-emerson and S. Plotkin, The neurofibromatoses. Part 2: NF2 and schwannomatosis, Rev Neurol Dis, vol.6, pp.81-86, 2009.

T. Hulsebos, A. Plomp, R. Wolterman, E. Robanus-maandag, F. Baas et al., Germline Mutation of INI1/SMARCB1 in Familial Schwannomatosis, The American Journal of Human Genetics, vol.80, issue.4, pp.805-810, 2007.
DOI : 10.1086/513207

K. Hadfield, W. Newman, N. Bowers, A. Wallace, C. Bolger et al., Molecular characterisation of SMARCB1 and NF2 in familial and sporadic schwannomatosis, Journal of Medical Genetics, vol.45, issue.6, pp.332-339, 2008.
DOI : 10.1136/jmg.2007.056499

C. Bacci, R. Sestini, A. Provenzano, I. Paganini, I. Mancini et al., Schwannomatosis associated with multiple meningiomas due to a familial SMARCB1 mutation, neurogenetics, vol.27, issue.1, pp.73-80, 2010.
DOI : 10.1007/s10048-009-0204-2

K. Hadfield, M. Smith, D. Trump, W. Newman, and D. Evans, SMARCB1 mutations are not a common cause of multiple meningiomas, Journal of Medical Genetics, vol.47, issue.8, pp.567-568, 2010.
DOI : 10.1136/jmg.2009.075721

URL : https://hal.archives-ouvertes.fr/hal-00557387

M. Maccollin, E. Chiocca, D. Evans, J. Friedman, R. Horvitz et al., Diagnostic criteria for schwannomatosis, Neurology, vol.64, issue.11, pp.1838-1845, 2005.
DOI : 10.1212/01.WNL.0000163982.78900.AD

C. Boyd, M. Smith, L. Kluwe, A. Balogh, M. Maccollin et al., Alterations in the SMARCB1 (INI1) tumor suppressor gene in familial schwannomatosis, Clinical Genetics, vol.56, issue.3Suppl, pp.358-366, 2008.
DOI : 10.1111/j.1399-0004.2008.01060.x

T. Hulsebos, S. Kenter, M. Jakobs, F. Baas, B. Chong et al., maternal germ line mosaicism in schwannomatosis, Clinical Genetics, vol.98, issue.1, pp.86-91, 2010.
DOI : 10.1111/j.1399-0004.2009.01249.x

R. Sestini, C. Bacci, A. Provenzano, M. Genuardi, and L. Papi, in schwannomatosis-associated schwannomas, Human Mutation, vol.394, issue.2, pp.227-231, 2008.
DOI : 10.1002/humu.20679

I. Christiaans, S. Kenter, H. Brink, T. Van-os, F. Baas et al., Germline SMARCB1 mutation and somatic NF2 mutations in familial multiple meningiomas, Journal of Medical Genetics, vol.48, issue.2, 2010.
DOI : 10.1136/jmg.2010.082420

URL : https://hal.archives-ouvertes.fr/hal-00573999

M. Smith, C. Boyd, M. Maccollin, and S. Plotkin, Identity analysis of schwannomatosis kindreds with recurrent constitutional SMARCB1 (INI1) alterations, Clin Genet, vol.75, pp.501-502, 2009.

. Rousseau, Cite this article as SMARCB1/INI1 germline mutations contribute to 10% of sporadic schwannomatosis, BMC Neurology, vol.11, issue.9, 2011.