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Open Access Research article

SMARCB1/INI1 germline mutations contribute to 10% of sporadic schwannomatosis

Guillaume Rousseau, Tetsuro Noguchi, Violaine Bourdon, Hagay Sobol and Sylviane Olschwang*

BMC Neurology 2011, 11:9  doi:10.1186/1471-2377-11-9

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