APA (7th ed.) Citation

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

Chicago Style (17th ed.) Citation

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

MLA (9th ed.) Citation

Hassan Vahidnezhad, et al. Lipoid Proteinosis Due to Homozygous Deletion Mutation (c.735delTG) in the ECM1 Gene Presents with Seizures and Hoarseness but No Skin Involvement. Wolters Kluwer Health, 2020.