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APA Citation
Spurlock, G., Bennett, E., Chuzhanova, N., Thomas, N., Jim, H., Side, L., Davies, S., Haan, E., Kerr, B., Huson, S. M., & Upadhyaya, M. (2009). sPRED1 mutations (Legius syndrome): another clinically useful genotype for dissecting the neurofibromatosis type 1 phenotype. Journal of medical genetics, 46(7), 431–437. http://access.bl.uk/ark:/81055/vdc_100137794646.0x000046