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

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ژورنال

عنوان ژورنال: Nature Genetics

سال: 2014

ISSN: 1061-4036,1546-1718

DOI: 10.1038/ng.2969