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HARVARD Citation
Khan, M. et al. (2019). Cost‐effective molecular inversion probe‐based ABCA4 sequencing reveals deep‐intronic variants in Stargardt disease. Human mutation. 40 (10), pp. 1749-1759. [Online].
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Khan, M. et al. (2019). Cost‐effective molecular inversion probe‐based ABCA4 sequencing reveals deep‐intronic variants in Stargardt disease. Human mutation. 40 (10), pp. 1749-1759. [Online].