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HARVARD Citation
Pasmant, E. et al. (2009). SPRED1 germline mutations caused a neurofibromatosis type 1 overlapping phenotype. Journal of medical genetics. 46 (7), pp. 425-430. [Online].
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Pasmant, E. et al. (2009). SPRED1 germline mutations caused a neurofibromatosis type 1 overlapping phenotype. Journal of medical genetics. 46 (7), pp. 425-430. [Online].