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HARVARD Citation
Nguyen, K. et al. (2017). A neurodevelopmental disorder with a nonsense mutation in the Ox-2 antigen domain of the amyloid precursor protein (APP) gene. Nucleosides, nucleotides & nucleic acids. pp. 317-327. [Online].
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Nguyen, K. et al. (2017). A neurodevelopmental disorder with a nonsense mutation in the Ox-2 antigen domain of the amyloid precursor protein (APP) gene. Nucleosides, nucleotides & nucleic acids. pp. 317-327. [Online].