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3), leading to the production of aberrant mRNAs. No other pathogenic variants in NMNAT1 have been previously shown to cause non-syndromic LCA. However, no patient with null biallelic variants has ever been described, and murine Nmnat1 knockouts show embryonic lethality. We hypothesize that complete absence of NMNAT1 activity is not compatible with life. The rearrangement found in our cases, presumably causing a strong but not complete reduction of enzymatic activity, may therefore result in an intermediate syndromic phenotype, between n
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