Detection of Hunter syndrome (mucopolysaccharidosis type II) in Taiwanese: biochemical and linkage studies of the iduronate-2-sulfatase gene defects in MPS II patients and carriers.

MLA

Lin, Shuan-Pei, et al. “Detection of Hunter Syndrome (Mucopolysaccharidosis Type II) in Taiwanese: Biochemical and Linkage Studies of the Iduronate-2-Sulfatase Gene Defects in MPS II Patients and Carriers.” Clinica Chimica Acta; International Journal of Clinical Chemistry, vol. 369, no. 1, July 2006, pp. 29–34. EBSCOhost, https://doi.org/10.1016/j.cca.2006.01.001.

APA

Lin, S.-P., Chang, J.-H., Lee-Chen, G.-J., Lin, D.-S., Lin, H.-Y., & Chuang, C.-K. (2006). Detection of Hunter syndrome (mucopolysaccharidosis type II) in Taiwanese: biochemical and linkage studies of the iduronate-2-sulfatase gene defects in MPS II patients and carriers. Clinica Chimica Acta; International Journal of Clinical Chemistry, 369(1), 29–34. https://doi.org/10.1016/j.cca.2006.01.001

Chicago

Lin, Shuan-Pei, Jui-Hung Chang, Guey-Jen Lee-Chen, Dar-Shong Lin, Hsiang-Yu Lin, and Chih-Kuang Chuang. 2006. “Detection of Hunter Syndrome (Mucopolysaccharidosis Type II) in Taiwanese: Biochemical and Linkage Studies of the Iduronate-2-Sulfatase Gene Defects in MPS II Patients and Carriers.” Clinica Chimica Acta; International Journal of Clinical Chemistry 369 (1): 29–34. doi:10.1016/j.cca.2006.01.001.