Search Results - Morteza Pishnamazi

  • Showing 1 - 1 results of 1
Refine Results
  1. 1
    Cover Image

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

    Published 2020
    Connect to this object online.
    Book

    Save to List
    Saved in:

Search Tools: