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                                       Details for article 2 of 12 found articles
 
 
  A novel homozygous mutation in SZT2 gene in Saudi family with developmental delay, macrocephaly and epilepsy
 
 
Title: A novel homozygous mutation in SZT2 gene in Saudi family with developmental delay, macrocephaly and epilepsy
Author: Naseer, Muhammad Imran
Alwasiyah, Mohammad Khalid
Abdulkareem, Angham Abdulrahman
Bajammal, Rayan Abdullah
Trujillo, Carlos
Abu-Elmagd, Muhammad
Jafri, Mohammad Alam
Chaudhary, Adeel G.
Al-Qahtani, Mohammad H.
Appeared in: Genes & genomics
Paging: Volume 40 (2018) nr. 11 pages 1149-1155
Year: 2018
Contents:
Publisher: The Genetics Society of Korea, Seoul
Source file: Elektronische Wetenschappelijke Tijdschriften
 
 

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