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

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Bibliographic Details
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.
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Call Number:	A1234.567
Copy 1	Available