Cite
HARVARD Citation
Umair, M. et al. (2018). Homozygous XYLT2 variants as a cause of spondyloocular syndrome. Clinical genetics. 93 (4), pp. 913-918. [Online].
This is an interim version of our Electronic Legal Deposit Catalogue-eJournals and eBooks while we continue to recover from a cyber-attack.
Umair, M. et al. (2018). Homozygous XYLT2 variants as a cause of spondyloocular syndrome. Clinical genetics. 93 (4), pp. 913-918. [Online].