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Synaptic Specificity, Recognition Molecules, and Assembly of Neural Circuits.
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Disease-associated mutations in human TUBB3 disturb netrin repulsive signaling.
PLoS One. 2019 Jun 21;14(6):e0218811. doi: 10.1371/journal.pone.0218811. eCollection 2019.
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Decreased ACKR3 (CXCR7) function causes oculomotor synkinesis in mice and humans.
Hum Mol Genet. 2019 Sep 15;28(18):3113-3125. doi: 10.1093/hmg/ddz137.
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Emerging roles of atypical chemokine receptor 3 (ACKR3) in normal development and physiology.
Cytokine. 2018 Sep;109:17-23. doi: 10.1016/j.cyto.2018.02.024.
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Recessive MYF5 Mutations Cause External Ophthalmoplegia, Rib, and Vertebral Anomalies.
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