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1. SPRED1 germline mutations caused a neurofibromatosis type 1 overlapping phenotype

Author

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., and France, R.N.F.

Subjects
Neurofibromatosis -- Research, Neurofibromatosis -- Genetic aspects, Phenotype -- Research, Phenotype -- Physiological aspects, Gene mutations -- Research, Health
Published
2009

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