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      Gain-of-Function Mutations in RIT1 Cause Noonan Syndrome, a RAS/MAPK Pathway Syndrome

      The American Journal of Human Genetics
      Elsevier BV

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          Journal
          10.1016/j.ajhg.2013.05.021
          https://www.elsevier.com/tdm/userlicense/1.0/

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