Cite
HARVARD Citation
Weisschuh, N. et al. (2020). Deep‐intronic variants in CNGB3 cause achromatopsia by pseudoexon activation. Human mutation. 41 (1), pp. 255-264. [Online].
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Weisschuh, N. et al. (2020). Deep‐intronic variants in CNGB3 cause achromatopsia by pseudoexon activation. Human mutation. 41 (1), pp. 255-264. [Online].