Mutations in RIT1 cause Noonan syndrome – additional functional evidence and expanding the clinical phenotype
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I. Mihalek | K. Gripp | G. Shi | D. Andres | O. Bodamer | Z Zhang | K. Sol‐Church | P. Rusconi | K W Gripp | I Mihalek | M Koenighofer | C Y Hung | J L McCauley | J Dallman | E J Back | K Sol-Church | P Rusconi | G-X Shi | D A Andres | O A Bodamer | J. Dallman | J. McCauley | M. Koenighofer | C. Hung | E. Back | Z. Zhang
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