Khan, Naz

Mutations in PRDM5 in Brittle Cornea Syndrome Identify a Pathway Regulating Extracellular Matrix Development and Maintenance

Burkitt Wright, E. M. M., Spencer, H. L., Daly, S. B., Manson, F. D. C., Zeef, L. A. H., Urquhart, J., Zoppi, N., Bonshek, R., Tosounidis, I., Mohan, M., et al. (2011) · The American Journal of Human Genetics

Corneal surgery and disordersConnective tissue disorders research

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Patient-facing genetic and genomic mobile apps in the UK: a systematic review of content, functionality, and quality

Gasteiger, N., Vercell, A., Davies, A., Dowding, D., Khan, N., & Davies, A. (2022) · Journal of Community Genetics

Mobile Health and mHealth ApplicationsHealth, Technology, Consumer Behavior

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