A case of Schopf-Schulz-Passarge syndrome caused by c.1135C > T WNT10A missense mutation

作者:Painsi Clemens*; Aubell Kristina; Wolf Peter; Hugel Rainer; Lange Asschenfeldt Bernhard
来源:Journal der Deutschen Dermatologischen Gesellschaft, 2017, 15(4): 454-456.
DOI:10.1111/ddg.13183