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

SMARCB1 mutations are not a common cause of multiple meningiomas

(2010) K. D. Hadfield et al.   JOURNAL OF MEDICAL GENETICS

Alterations in the SMARCB1 (INI1) tumor suppressor gene in familial schwannomatosis

(2009) C Boyd et al.   CLINICAL GENETICS

Four novelSPG3A/atlastinmutations identified in autosomal dominant hereditary spastic paraplegia kindreds with intra-familial variability in age of onset and complex phenotype

(2009) BN Smith et al.   CLINICAL GENETICS

SMARCB1/INI1maternal germ line mosaicism in schwannomatosis

(2009) TJM Hulsebos et al.   CLINICAL GENETICS

Schwannomatosis associated with multiple meningiomas due to a familial SMARCB1 mutation

(2009) Costanza Bacci et al.   NEUROGENETICS

Evidence of a four-hit mechanism involvingSMARCB1andNF2in schwannomatosis-associated schwannomas

(2007) Roberta Sestini et al.   HUMAN MUTATION