Order Article Reprints

Sheikh TI, Harripaul R, Vasli N, Ghadami M, Santangelo SL, Ayub M, Sasanfar R, Vincent JB. Heterozygous De Novo Truncating Mutation of Nucleolin in an ASD Individual Disrupts Its Nucleolar Localization. Genes. 2022; 13(1):51. https://doi.org/10.3390/genes13010051

Sheikh, Taimoor I., Ricardo Harripaul, Nasim Vasli, Majid Ghadami, Susan L. Santangelo, Muhammad Ayub, Roksana Sasanfar, and John B. Vincent. 2022. "Heterozygous De Novo Truncating Mutation of Nucleolin in an ASD Individual Disrupts Its Nucleolar Localization" Genes 13, no. 1: 51. https://doi.org/10.3390/genes13010051

Sheikh, T. I., Harripaul, R., Vasli, N., Ghadami, M., Santangelo, S. L., Ayub, M., Sasanfar, R., & Vincent, J. B. (2022). Heterozygous De Novo Truncating Mutation of Nucleolin in an ASD Individual Disrupts Its Nucleolar Localization. Genes, 13(1), 51. https://doi.org/10.3390/genes13010051