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HARVARD Citation
Heimer, G. et al. (2020). Netrin‐G2 dysfunction causes a Rett‐like phenotype with areflexia. Human mutation. 41 (2), pp. 476-486. [Online].
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Heimer, G. et al. (2020). Netrin‐G2 dysfunction causes a Rett‐like phenotype with areflexia. Human mutation. 41 (2), pp. 476-486. [Online].