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Smith, M. et al. (2020). A deep intronic SMARCB1 variant associated with schwannomatosis. Clinical genetics. 97 (2), pp. 376-377. [Online].
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Smith, M. et al. (2020). A deep intronic SMARCB1 variant associated with schwannomatosis. Clinical genetics. 97 (2), pp. 376-377. [Online].