Noonan syndrome in diverse populations

• Main Authors: Kruszka P., Porras A., Addissie Y., Moresco A., Medrano S., Mok G., Leung G., Tekendo-Ngongang C., Uwineza A., Thong M., Muthukumarasamy P., Honey E., Ekure E., Sokunbi O., Kalu N., Jones K., Kaplan J., Abdul-Rahman O., Vincent L., Love A., Belhassan K., Ouldim K., El Bouchikhi I., Shukla A., Girisha K., Patil S., Sirisena N., Dissanayake V., Paththinige C., Mishra R., Klein-Zighelboim E., Gallardo Jugo B., Chávez Pastor M., Abarca-Barriga H., Skinner S., Prijoles E., Badoe E., Gill A., Shotelersuk V., Smpokou P., Kisling M., Ferreira C., Mutesa L., Megarbane A., Kline A., Kimball A., Okello E., Lwabi P., Aliku T., Tenywa E., Boonchooduang N., Tanpaiboon P., Richieri-Costa A., Wonkam A., Chung B., Stevenson R., Summar M., Mandal K., Phadke S., Obregon M., Linguraru M., Muenke M.
• Format: Journal
• Published: 2017
• Online Access: https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85026314237&origin=inward; http://cmuir.cmu.ac.th/jspui/handle/6653943832/40160
• Institution: Chiang Mai University

© 2017 Wiley Periodicals, Inc. Noonan syndrome (NS) is a common genetic syndrome associated with gain of function variants in genes in the Ras/MAPK pathway. The phenotype of NS has been well characterized in populations of European descent with less attention given to other groups. In this study, in...