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Homocarnosinosis: A historical update and findings in the SPG11 gene.
Sjaastad O, Blau N, Rydning SL, Peters V, Rødningen O, Stray-Pedersen A, Krossnes B, Tallaksen C, Koht J. Sjaastad O, et al. Among authors: rodningen o. Acta Neurol Scand. 2018 Sep;138(3):245-250. doi: 10.1111/ane.12949. Epub 2018 May 6. Acta Neurol Scand. 2018. PMID: 29732542
Phenotypic consequences of a deletion of exons 2 and 3 of the LDL receptor gene.
Rødningen OK, Tonstad S, Medh JD, Chappell DA, Ose L, Leren TP. Rødningen OK, et al. J Lipid Res. 1999 Feb;40(2):213-20. J Lipid Res. 1999. PMID: 9925649 Free article.
Possible mechanisms for this phenotypic variability are discussed.-Rodningen, O. K., S. Tonstad, J. D. Medh, D. A. Chappell, L. Ose, and T. ...
Possible mechanisms for this phenotypic variability are discussed.-Rodningen, O. K., S. Tonstad, J. D. Medh, D. A. Chappell, L …
Molecular genetics of familial hypercholesterolaemia in Norway.
Leren TP, Tonstad S, Gundersen KE, Bakken KS, Rødningen OK, Sundvold H, Ose L, Berg K. Leren TP, et al. Among authors: rodningen ok. J Intern Med. 1997 Mar;241(3):185-94. doi: 10.1046/j.1365-2796.1997.78119000.x. J Intern Med. 1997. PMID: 9104431 Free article.
58 results