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Poulter, JA and Al-Araimi, M and Conte, I and Van Genderen, MM and Sheridan, E and Carr, IM and Parry, DA and Shires, M and Carrella, S and Bradbury, J and Khan, K and Lakeman, P and Sergouniotis, PI and Webster, AR and Moore, AT and Pal, B and Mohamed, MD and Venkataramana, A and Ramprasad, V and Shetty, R and Saktivel, M and Kumaramanickavel, G and Tan, A and Mackey, DA and Hewitt, AW and Banfi, S and Ali, M and Inglehearn, CF and Toomes, C, “Recessive mutations in SLC38a8 cause foveal hypoplasia and optic nerve misrouting without albinism”, American Journal of Human Genetics: A Record of Research, Review and Bibliographic Material Relating to Heredity in Man, 93 (6) pp. 1143-1150. ISSN 0002-9297 (2013) [Refereed Article]
Data TypeValue
Type of ResearchStrategic Basic Research
Research DivisionMedical and Health Sciences
Research GroupOphthalmology and Optometry
Research FieldOphthalmology
Research Objective DivisionHealth
Research Objective GroupClinical Health (Organs, Diseases and Abnormal Conditions)
Research Objective FieldHearing, Vision, Speech and Their Disorders
Visit Item on eCitehttp://ecite.utas.edu.au/95028
Digital Object Identifierdoi:10.1016/j.ajhg.2013.11.002
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Number of Times Cited31