Cite

    Wu, H., Ren, X., Ge, M., Dong, P., Wang, S., Yi, H., Li, X., Huo, J., Zheng, X., Gao, M., Huang, J., Zhang, J., Wang, M., Jin, P., Nie, N., Shao, Y., & Zheng, Y. (2022). the novel SLC40A1 (T419I) variant results in a loss-of-function phenotype and may provide insights into the mechanism of large granular lymphocytic leukemia and pure red cell aplasia. Blood science, 4(1), 29–37. http://access.bl.uk/ark:/81055/vdc_100150610964.0x00000c