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APA Citation
Busa, T., Milh, M., Degardin, N., Girard, N., Sigaudy, S., Longy, M., Olshchwang, S., Sobol, H., Chabrol, B., & Philip, N. (n.d.). clinical presentation of PTEN mutations in childhood in the absence of family history of Cowden syndrome. European journal of paediatric neurology, 19, 188–192. http://access.bl.uk/ark:/81055/vdc_100051528828.0x00003c