Order Article Reprints

Stanke F, Becker T, Ismer HS, Dunsche I, Hedtfeld S, Kontsendorn J, Dittrich A-M, Tümmler B. Consistent Assignment of Risk and Benign Allele at rs2303153 in the CF Modifier Gene SCNN1B in Three Independent F508del-CFTR Homozygous Patient Populations. Genes. 2021; 12(10):1554. https://doi.org/10.3390/genes12101554

Stanke, Frauke, Tim Becker, Haide Susanne Ismer, Inga Dunsche, Silke Hedtfeld, Julia Kontsendorn, Anna-Maria Dittrich, and Burkhard Tümmler. 2021. "Consistent Assignment of Risk and Benign Allele at rs2303153 in the CF Modifier Gene SCNN1B in Three Independent F508del-CFTR Homozygous Patient Populations" Genes 12, no. 10: 1554. https://doi.org/10.3390/genes12101554

Stanke, F., Becker, T., Ismer, H. S., Dunsche, I., Hedtfeld, S., Kontsendorn, J., Dittrich, A.-M., & Tümmler, B. (2021). Consistent Assignment of Risk and Benign Allele at rs2303153 in the CF Modifier Gene SCNN1B in Three Independent F508del-CFTR Homozygous Patient Populations. Genes, 12(10), 1554. https://doi.org/10.3390/genes12101554