9z7s | pdb_00009z7s
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Human NIPA2 mutant A75T
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Structural highlights
DiseaseNIPA2_HUMAN 15q11.2 microdeletion syndrome. FunctionNIPA2_HUMAN Acts as a selective Mg(2+) transporter.[1] References
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This page was last modified 20:35, 29 July 2026.