The Fourth International Symposium on Genetic Disorders of the Ras/MAPK pathway
- Stevenson, D.A. (David A.)
- Schill, L. (Lisa)
- Schoyer, L. (Lisa)
- Andresen, B.S. (B.)
- Bakker, A. (Annette)
- Bayrak-Toydemir, P. (Pinar)
- Burkitt Wright, E.M.M. (Emma M.)
- Chatfield, K. (Kathryn)
- Elefteriou, F. (Florent)
- Elgersma, Y. (Ype)
- Fisher, M.J. (Michael J.)
- Franz, D. (David)
- Gelb, B.D. (Bruce)
- Goriely, A. (Anne)
- Gripp, K.W. (Karen)
- Hardan, A.Y. (Antonio Y.)
- Keppler-Noreuil, K.M. (Kim M.)
- Kerr, B. (Bronwyn)
- Korf, B. (Bruce)
- Leoni, C. (Chiara)
- Mccormick, F. (Frank)
- Plotkin, S.R. (Scott R.)
- Rauen, K.A. (Katherine)
- Reilly, K. (Karlyne)
- Roberts, A.E.
- Sandler, A. (Abby)
- Siegel, D. (Dawn)
- Walsh, K.S. (Karin S.)
- Widemann, B.C. (Brigitte C.)
Publication date
August 2016
DOI Publisher
Wiley ISSN
1552-4825 Citation count (estimate)
2Abstract
The RASopathies are a group of disorders due to variations of genes associated with the Ras/MAPK pathway. Some of the RASopathies include neurofibromatosis type 1 (NF1), Noonan syndrome, Noonan syndrome with multiple lentigines, cardiofaciocutaneous (CFC) syndrome, Costello syndrome, Legius syndrome, and capillary malformation-arteriovenous malformation (CM-AVM) syndrome. In combination, the RASopathies are a frequent group of genetic disorders. This report summarizes the proceedings of the 4th International Symposium on Genetic Disorders of the Ras/MAPK pathway and highlights gaps in the field
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