Items where authors include "Kumaramanickavel, G"

Article

Poulter, JA, Al-Araimi, M, Conte, I et al. (26 more authors) (2013) Recessive Mutations in SLC38A8 Cause Foveal Hypoplasia and Optic Nerve Misrouting without Albinism. American Journal of Human Genetics, 93 (6). 1143 - 1150. ISSN 0002-9297

Ramprasad, VL, Soumittra, N, Nancarrow, D et al. (7 more authors) (2008) Identification of a novel splice-site mutation in the Lebercilin (LCA5) gene causing Leber congenital amaurosis. Molecular Vision, 10 (14). pp. 481-486. ISSN 1090-0535