Williams, Lloyd B. http://orcid.org/0000-0002-7285-0253
Javed, Asif
Sabri, Amin
Morgan, Denise J.
Huff, Chad D.
Grigg, John R.
Heng, Xiu Ting
Khng, Alexis J.
Hollink, Iris H.I.M.
Morrison, Margaux A.
Owen, Leah A.
Anderson, Katherine
Kinard, Krista
Greenlees, Rebecca
Novacic, Danica
Nida Sen, H.
Zein, Wadih M.
Rodgers, George M.
Vitale, Albert T.
Haider, Neena B.
Hillmer, Axel M.
Ng, Pauline C.
Shankaracharya,
Cheng, Anson
Zheng, Linda
Gillies, Mark C.
van Slegtenhorst, Marjon
van Hagen, P. Martin
Missotten, Tom O.A.R.
Farley, Gary L.
Polo, Michael
Malatack, James
Curtin, Julie
Martin, Frank
Arbuckle, Susan
Alexander, Stephen I.
Chircop, Megan
Davila, Sonia
Digre, Kathleen B.
Jamieson, Robyn V.
DeAngelis, Margaret M.
Funding for this research was provided by:
National Health and Medical Research Council (1099165)
A*STAR JCO (Career Development Grant)
Research to Prevent Blindness (Department of Ophthalmology and Visual Sciences, Moran Eye Centre, University of Utah)
This article is maintained by: Elsevier
Article Title: ALPK1 missense pathogenic variant in five families leads to ROSAH syndrome, an ocular multisystem autosomal dominant disorder
Journal Title: Genetics in Medicine
CrossRef DOI link to publisher maintained version: https://doi.org/10.1038/s41436-019-0476-3
Content Type: article
Copyright: © 2019, The Author(s), under exclusive licence to the American College of Medical Genetics and Genomics