SPRED1 germline mutations caused a neurofibromatosis type 1 overlapping phenotype.
Pasmant, E.; Sabbagh, A.; Hanna, N.; Masliah-Planchon, J.; Jolly, E.; Goussard, P.; Ballerini, P.; Cartault, F.; Barbarot, S.; Landman-Parker, J.; Soufir, N.; Parfait, B.; Vidaud, M.; Wolkenstein, P.; Vidaud, D.; France, R. N. F.; Journal of Medical Genetics, 2009, vol. 46, issue 7, p 1, ISSN 00222593. ISBN 14686244.

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