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HARVARD Citation
Batzios, S. et al. (2022). Newly identified disorder of copper metabolism caused by variants in CTR1, a high-affinity copper transporter. Human molecular genetics. 31 (24), pp. 4121-4130. [Online].
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Batzios, S. et al. (2022). Newly identified disorder of copper metabolism caused by variants in CTR1, a high-affinity copper transporter. Human molecular genetics. 31 (24), pp. 4121-4130. [Online].