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Diversity of the basic defect of homozygous CFTR mutation genotypes in humans.
Stanke F, Ballmann M, Bronsveld I, Dörk T, Gallati S, Laabs U, Derichs N, Ritzka M, Posselt HG, Harms HK, Griese M, Blau H, Mastella G, Bijman J, Veeze H, Tümmler B. Stanke F, et al. Among authors: laabs u. J Med Genet. 2008 Jan;45(1):47-54. doi: 10.1136/jmg.2007.053561. J Med Genet. 2008. PMID: 18178635 Free article.
Genes that determine immunology and inflammation modify the basic defect of impaired ion conductance in cystic fibrosis epithelia.
Stanke F, Becker T, Kumar V, Hedtfeld S, Becker C, Cuppens H, Tamm S, Yarden J, Laabs U, Siebert B, Fernandez L, Macek M Jr, Radojkovic D, Ballmann M, Greipel J, Cassiman JJ, Wienker TF, Tümmler B. Stanke F, et al. Among authors: laabs u. J Med Genet. 2011 Jan;48(1):24-31. doi: 10.1136/jmg.2010.080937. Epub 2010 Sep 12. J Med Genet. 2011. PMID: 20837493 Free PMC article.