Novel familial KDF1 mutation detected in members of a three-generation family with clinical manifestations of ectodermal dysplasia: A report of four cases
Biomed Rep. 2025 May 21;23(1):121. doi: 10.3892/br.2025.1999. eCollection 2025 Jul. ABSTRACT Ectodermal dysplasia (ED) syndromes are a heterogeneous group of disorders characterized by defects in …