Lipoid Proteinosis Due to Homozygous Deletion Mutation (c.735delTG) in the ECM1 Gene Presents with Seizures and Hoarseness but No Skin Involvement

• Main Authors: Hassan Vahidnezhad (Author), Leila Youssefian (Author), Abbas Tafakhori (Author), Qiaoli Li (Author), Jouni Uitto (Author), Fatemeh Vand Rajabpour (Author), Morteza Pishnamazi (Author), Amirhossein Modabbernia (Author), Mina Tabrizi (Author)
• Format: Book
• Published: Wolters Kluwer Health, 2020-03-01T00:00:00Z.
• Subjects: article
• Online Access: Connect to this object online.

Item Description

2096-5540
2641-8746
10.1097/JD9.0000000000000056