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A recurrent neomorphic mutation in MYOD1 defines a clinically aggressive subset of embryonal rhabdomyosarcoma associated with PI3K-AKT pathway mutations

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Description scientific article
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author: Marc Ladanyi  Raf Sciot  Leonard H Wexler  Frederic G. Barr  Samuel Singer  Jorge Reis-Filho  Paul Meyers  Charlotte K Y Ng 

Publication date May 4, 2014
Language English
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