Structural modeling of a novel SLC38A8 mutation that causes foveal hypoplasia
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DOI: 10.1002/mgg3.266
Abstract: Foveal hypoplasia (FH) in the absence of albinism, aniridia, microphthalmia, or achromatopsia is exceedingly rare, and the molecular basis for the disorder remains unknown. FH is characterized by the absence of both the retinal foveal… read more here.
Keywords: modeling novel; novel slc38a8; structural modeling; foveal hypoplasia ... See more keywords