Barely Significant
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Leber's Hereditary Optic Neuropathy-Specific Heteroplasmic Mutation m.14495A>G Found in a Chinese Family.

Transl Vis Sci Technol · 2019 · PMC6615366 · PMID 31316863

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However, in the current study, carriers versus affected did not reach statistical significance ( Supplementary Fig.

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