Cite
MLA Citation
G Spurlock et al.. “SPRED1 mutations (Legius syndrome): another clinically useful genotype for dissecting the neurofibromatosis type 1 phenotype.” Journal of medical genetics, vol. 46, no. 7, 2009, pp. 431–437. http://access.bl.uk/ark:/81055/vdc_100137794646.0x000046