Familial Chilblain Lupus – A Monogenic Form of Cutaneous Lupus Erythematosus due to a Heterozygous Mutation in TREX1

by Günther, Claudia, Meurer, Michael, Stein, Annette, Viehweg, Antje, Lee-Kirsch, Min-Ae
Published 2014

Phenotypic Variability in a Family with Aicardi-Goutières Syndrome Due to the Common A177T RNASEH2B Mutation

by Tüngler, Victoria, Schmidt, Franziska, Hieronimus, Steve, Reyes-Velasco, Claudio, Lee-Kirsch, Min Ae
Published 2014

Assignment of the human homeobox 11-like 2 gene (HOX11L2) to chromosome 5q34→q35 by radiation hybrid mapping

by Lee-Kirsch, Min-Ae, Engel, Kerstin, Paditz, Ekkehart, Rösen-Wolff, Angela, Lee, Young-Ae, Gahr, Manfred
Published 2014