Cite
MLA Citation
M. Umair et al.. “Homozygous XYLT2 variants as a cause of spondyloocular syndrome.” Clinical genetics, vol. 93, no. 4, 2018, pp. 913–918. http://access.bl.uk/ark:/81055/vdc_100057591985.0x000042
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M. Umair et al.. “Homozygous XYLT2 variants as a cause of spondyloocular syndrome.” Clinical genetics, vol. 93, no. 4, 2018, pp. 913–918. http://access.bl.uk/ark:/81055/vdc_100057591985.0x000042