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Research Output Details
| 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 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/95028 |
| Digital Object Identifier | doi:10.1016/j.ajhg.2013.11.002 |
| 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 | 61 |