Condition: NOONAN SYNDROME 9


rs1442962879 in SOS2 gene and NOONAN SYNDROME 9 PMID 25795793 2015 Rare variants in SOS2 and LZTR1 are associated with Noonan syndrome.

PMID 26173643 2015 Activating Mutations Affecting the Dbl Homology Domain of SOS2 Cause Noonan Syndrome.