IndraLab

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"For example, NS is associated with mutations in A2ML1 , CBL , KRAS , LZTR1 , MAP3K8 , MYST4 , NRAS , PTPN11 , RAF1 , RASA2 , RRAS , RIT1 , SHOC2 , SOS1 , SOS2 and SPRY1 , whereas mutations in HRAS and SPRED1 have been described for CS and Legius syndrome, respectively ( xref ; xref , xref )."