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Z., Loizidou, M., Ahmed, M

As for genetic and pathology of MPNST, recurrent genetic mutations have been identified in recent studies, such as loss-of function in NF1 , PRC2 , TP53 , CDKN2A , which may provide new opportunities for therapeutic intervention [21]

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Le Glutathion a une double origine et on le retrouve la fois dans les cellules vgtales et animales

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