Two novel germline KRAS mutations: expanding the molecular and clinical phenotype
Z Stark, G Gillessen-Kaesbach, MM Ryan, IC Cirstea, L Gremer, MR Ahmadian, R Savarirayan, M Zenker
Clinical Genetics | WILEY-BLACKWELL | Published : 2012
We thank the families for their participation in the research. This work was supported by grants from the European Research Area Network for research programmes on rare diseases (E-Rare) 2009 to M. Z. and M. R. A. (European Network on Noonan Syndrome and Related Disorders).