Hasil Pencarian - Mohammed Z. Seidahmed

  • Menampilkan 1 - 3 hasil dari 3
Perbaiki Hasil
  1. 1
    GABA transaminase deficiency. Case report and literature review

    GABA transaminase deficiency. Case report and literature review oleh Amira Oshi, Abdullah Alfaifi, Mohammed Z. Seidahmed, Khalid Al Hussein, Abeer Miqdad, Abdelmohsin Samadi, Omar Abdelbasit

    Diterbitkan 2021-03-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  2. 2
    Ancient founder mutation in RUBCN: a second unrelated family confirms Salih ataxia (SCAR15)

    Ancient founder mutation in RUBCN: a second unrelated family confirms Salih ataxia (SCAR15) oleh Mohammed Z. Seidahmed, Muddathir H. Hamad, Albandary AlBakheet, Salah A. Elmalik, Abdulmajeed AlDrees, Jumanah Al-Sufayan, Ibrahim Alorainy, Ibrahim M. Ghozzi, Dilek Colak, Mustafa A. Salih, Namik Kaya

    Diterbitkan 2020-05-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  3. 3
    Mutation in GM2A Leads to a Progressive Chorea-Dementia Syndrome

    Mutation in GM2A Leads to a Progressive Chorea-Dementia Syndrome oleh Mustafa A. Salih, Mohammed Z. Seidahmed, Heba Y. El Khashab, Muddathir H. Hamad, Thomas M. Bosley, Sabrina Burn, Angela Myers, Megan L. Landsverk, Patricia L. Crotwell, Kaya Bilguvar, Shrikant Mane, Michael C. Kruer

    Diterbitkan 2015-07-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:

Alat Pencarian: