Search Results - Naghmeh Gholipour

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

    A novel start-loss mutation of the SLC29A3 gene in a consanguineous family with H syndrome: clinical characteristics, in silico analysis and literature review by Nahid Rezaie, Nader Mansour Samaei, Ayda Ghorbani, Naghmeh Gholipour, Shohreh Vosough, Mahboobeh Rafigh, Abolfazl Amini

    Published 2024
    Connect to this object online.
    Book

    Save to List
    Saved in:

Search Tools: