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

Callea, M.Nieminen, P.Willoughby, C. E.Clarich, G.Yavuz, I.Vinciguerra, A.Di Stazio, M.2024-04-242024-04-2420160926-99591468-3083https://doi.org/10.1111/jdv.12747https://hdl.handle.net/11468/17687[Abstract Not Available]eninfo:eu-repo/semantics/openAccess[No Keyword]A novel INDEL mutation in the EDA gene resulting in a distinct X- linked hypohidrotic ectodermal dysplasia phenotype in an Italian familyA novel INDEL mutation in the EDA gene resulting in a distinct X- linked hypohidrotic ectodermal dysplasia phenotype in an Italian familyLetter302341343WOS:0003689931000282-s2.0-849566906762526627210.1111/jdv.12747Q1Q1