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Research Output Details
| Khan, K and Rudkin, A and Parry, DA and Burdon, KP and McKibbin, M and Logan, CV and Abdelhamed, ZIA and Muecke, JS and Fernandez-Fuentes, N and Laurie, KJ and Shires, M and Fogarty, R and Carr, IM and Poulter, JA and Morgan, JE and Mohamed, MD and Jafri, H and Raashid, Y and Meng, N and Piseth, H and Toomes, C and Casson, RJ and Taylor, GR and Hammerton, M and Sheridan, E and Johnson, CA and Inglehearn, CF and Craig, JE and Ali, M, “Homozygous mutations in PXDN cause congenital cataract, corneal opacity, and developmental glaucoma”, American Journal of Human Genetics: A Record of Research, Review and Bibliographic Material Relating to Heredity in Man, 89 (3) pp. 464-473. ISSN 0002-9297 (2011) [Refereed Article] | |
| Data Type | Value |
|---|---|
| Type of Research | Strategic Basic Research |
| Research Division | Biomedical and Clinical Sciences |
| Research Group | Ophthalmology and optometry |
| Research Field | Ophthalmology |
| Research Objective Division | Health |
| Research Objective Group | Clinical health |
| Research Objective Field | Clinical health not elsewhere classified |
| Visit Item on eCite | http://ecite.utas.edu.au/90662 |
| Digital Object Identifier | doi:10.1016/j.ajhg.2011.08.005 |
| Scopus Source URL | View the full record on Scopus |
| Scopus Citing URL | View the list of citing articles on Scopus |
| Web of Science® Source URL | View the full record on Web of Science® |
| Web of Science® Citing URL | View the list of citing articles on Web of Science® |
| Web of Science® Related URL | View the list of related articles on Web of Science® |
| Number of Times Cited | 56 |