Konu "RD3 Mutation" için Makale Koleksiyonu listeleme
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Optical coherence tomography and fundus autofluorescence imaging in an infant with RD3-related leber congenital amaurosis
(Taylor and Francis Inc., 2020)Background: Leber congenital amaurosis (LCA) is both genetically and phenotypically heterogeneous group of retinal disorder. Mutations in retinal degeneration 3 (RD3) have been reported as an infrequent cause of LCA which ...