Mutations in <i><scp>RIT1</scp></i> cause Noonan syndrome – additional functional evidence and expanding the clinical phenotype
Martin Koenighofer(Medical University of Vienna), Olaf A. Bodamer(Broad Institute), Ivana Mihalek(Boston Children's Hospital), Paolo Rusconi(University of Miami), Katia Sol‐Church(Nemours Children’s Clinic), Jacob L. McCauley(University of Cambridge), Karen W. Gripp(Alfred I. duPont Hospital for Children), G‐X. Shi(University of Kentucky), Chia-Yang Hung(National Cheng Kung University), Elke Back(University of Miami), Julia E. Dallman(University of Miami), D. A. Andres(University of Kentucky), Z. Zhang(University of Kentucky)
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