A novel INDEL mutation in the EDA gene resulting in a distinct X- linked hypohidrotic ectodermal dysplasia phenotype in an Italian family

作者:Callea M*; Nieminen P; Willoughby C E; Clarich G; Yavuz I; Vinciguerra A; Di Stazio M; Giglio S; Sani I; Maglione M; Pensiero S; Tadini G; Bellacchio E
来源:Journal of the European Academy of Dermatology and Venereology, 2016, 30(2): 341-343.
DOI:10.1111/jdv.12747