Web Access Research Portal

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 TypeValue
Type of ResearchStrategic Basic Research
Research DivisionBiomedical and Clinical Sciences
Research GroupOphthalmology and optometry
Research FieldOphthalmology
Research Objective DivisionHealth
Research Objective GroupClinical health
Research Objective FieldClinical health not elsewhere classified
Visit Item on eCitehttp://ecite.utas.edu.au/90662
Digital Object Identifierdoi:10.1016/j.ajhg.2011.08.005
Scopus Source URLView the full record on Scopus
Scopus Citing URLView the list of citing articles on Scopus
Web of Science® Source URLView the full record on Web of Science®
Web of Science® Citing URLView the list of citing articles on Web of Science®
Web of Science® Related URLView the list of related articles on Web of Science®
Number of Times Cited55