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HARVARD Citation
Szczałuba, K. et al. (2018). Neurodevelopmental phenotype caused by a de novo PTPN4 single nucleotide variant disrupting protein localization in neuronal dendritic spines. Clinical genetics. 94 (6), pp. 581-585. [Online].
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Szczałuba, K. et al. (2018). Neurodevelopmental phenotype caused by a de novo PTPN4 single nucleotide variant disrupting protein localization in neuronal dendritic spines. Clinical genetics. 94 (6), pp. 581-585. [Online].