Mutations in RIT1 cause Noonan syndrome - additional functional evidence and expanding the clinical phenotype

M. Koenighofer, C. Y. Hung, J. L. Mccauley, J. Dallman, E. J. Back, I. Mihalek, K. W. Gripp, K. Sol-Church, P. Rusconi, Z. Zhang, G. X. Shi, D. A. Andres, O. A. Bodamer

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Medicine & Life Sciences