Lipoid Proteinosis Due to Homozygous Deletion Mutation (c.735delTG) in the ECM1 Gene Presents with Seizures and Hoarseness but No Skin Involvement - Hassan Vahidnezhad; Leila Youssefian; Abbas Tafakhori; Qiaoli Li; Jouni Uitto; Fatemeh Vand Rajabpour; Morteza Pishnamazi; Amirhossein Modabbernia; Mina Tabrizi (Wolters Kluwer Health, 2020)