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APA Citation
Bi, W., Glass, I. A., Muzny, D. M., Gibbs, R. A., Eng, C. M., Yang, Y., & Sun, A. (2016). whole exome sequencing identifies the first STRADA point mutation in a patient with polyhydramnios, megalencephaly, and symptomatic epilepsy syndrome (PMSE). American journal of medical genetics, 170(8), 2181–2185. http://access.bl.uk/ark:/81055/vdc_100034681256.0x00003a