Publication | Closed Access
Clinical and molecular characterization of non-syndromic retinal dystrophy due to c.175G>A mutation in ceroid lipofuscinosis neuronal 3 (CLN3)
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Citations
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References
2018
Year
Molecular CharacterizationOcular DiseaseMolecular NeuroscienceRetinaOphthalmologyPathologyDegenerative DiseaseNeurologyOcular PathologyChoroid PlexusNeuropathologyMedicineNon-syndromic Retinal DystrophyNeurogenetics
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