Stanke, F.; Becker, T.; Ismer, H.S.; Dunsche, I.; Hedtfeld, S.; Kontsendorn, J.; Dittrich, A.-M.; TĂĽmmler, 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, 1554.
https://doi.org/10.3390/genes12101554
AMA Style
Stanke F, Becker T, Ismer HS, Dunsche I, Hedtfeld S, Kontsendorn J, Dittrich A-M, TĂĽmmler 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
Chicago/Turabian Style
Stanke, Frauke, Tim Becker, Haide Susanne Ismer, Inga Dunsche, Silke Hedtfeld, Julia Kontsendorn, Anna-Maria Dittrich, and Burkhard TĂĽmmler.
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
APA Style
Stanke, F., Becker, T., Ismer, H. S., Dunsche, I., Hedtfeld, S., Kontsendorn, J., Dittrich, A.-M., & TĂĽmmler, 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