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Brems, H., Chmara, M., Sahbatou, M., Denayer, E., Taniguchi, K., Kato, R., Somers, R., Messiaen, L., De Schepper, S., Fryns, JP., Cools, J., Marynen, P., Thomas, G., Yoshimura, A. and Legius, E. (2007) Germline loss-of-function mutations in SPRED1 cause a neurofibromatosis 1-like phenotype. Nature Genetics, 39, 1120-1126. doi:10.1038/ng2113

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