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Lebers Congenital Amaurosis

Sept. 9, 2024

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Identified the NMNAT1 mutations as a cause of Leber congenital amaurosis (LCA), one…
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Leber Congenital Amaurosis
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DYNC2H1 variants cause Leber congenital amaurosis without syndromic features - Lee …
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RPE65-associated Leber Congenital Amaurosis. EyeRounds.org - Ophthalmology - The Un…
Review and update on the molecular basis of Leber congenital amaurosis
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Figure 8 from The phenotype of Leber congenital amaurosis in patients with AIPL1 mu…
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A Novel Mutation in the RPE65 Gene Causing Leber Congenital Amaurosis and Its Trans…
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Results at 2 Years after Gene Therapy for RPE65-Deficient Leber Congenital Amaurosi…
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