Cite
MLA Citation
Weimin Bi et al.. “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, vol. 170, no. 8, 2016, pp. 2181–2185. http://access.bl.uk/ark:/81055/vdc_100034681256.0x00003a