APPENDICES 248 P Katrine M. Johannesen, Yuanyuan Liu, Mahmoud Koko, Catherine E. Gjerulfsen, Lukas Sonnenberg, Julian Schubert, ….. Aster V.E. Harder ….. et al. Genotype-phenotype correlations in SCN8A-related disorders reveal prognostic and therapeutic implications. Brain. 2021 Aug 25:awab321. Sarah L. Gardiner, Aster V.E. Harder, Yvonne J.M. Campman, Stella Trompet, Jacobijn Gussekloo, Martine J. van Belzen, Merel W. Boogaard, Raymund A.C. Roos, et al. Repeat length variations in ATXN1 and AR modify disease expression in Alzheimer’s disease. Neurobiological Aging. 2019;73:230.e9-230.e17. Eduardo Calpena, Alexia Hervieu, Teresa Kaserer, Sigrid M.A. Swagemakers, Jaqueline A.C. Goos, Olajumoke Popoola, ….. Aster V.E. Harder ….. et al. De Novo Missense Substitutions in the Gene Encoding CDK8, a Regulator of the Mediator Complex, Cause a Syndromic Developmental Disorder. American Journal of Human Genetics 2019;104(4):709-720
RkJQdWJsaXNoZXIy MTk4NDMw