Search Results - Mahmoud Koko

  • Showing 1 - 2 results of 2
Refine Results
  1. 1
    Cover Image

    Case report: Novel SCN4A variant associated with a severe congenital myasthenic syndrome/myopathy phenotype by Veronika M. Berghold, Mahmoud Koko, Riccardo Berutti, Riccardo Berutti, Barbara Plecko

    Published 2022
    Connect to this object online.
    Book

    Save to List
    Saved in:
  2. 2
    Cover Image

    Case report of a novel homozygous splice site mutation in PLA2G6 gene causing infantile neuroaxonal dystrophy in a Sudanese family by Liena E. O. Elsayed, Inaam N. Mohammed, Ahlam A. A. Hamed, Maha A. Elseed, Mustafa A. M. Salih, Ashraf Yahia, Rayan A. Siddig, Mutaz Amin, Mahmoud Koko, Mustafa I. Elbashir, Muntaser E. Ibrahim, Alexis Brice, Ammar E. Ahmed, Giovanni Stevanin

    Published 2018
    Connect to this object online.
    Book

    Save to List
    Saved in:

Search Tools: