Works by Asifullah


Results: 104
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    Whole exome sequencing identifies a novel compound heterozygous GFM1 variant underlying developmental delay, dystonia, polymicrogyria, and severe intellectual disability in a Pakhtun family.

    Published in:
    American Journal of Medical Genetics. Part A, 2022, v. 188, n. 9, p. 2693, doi. 10.1002/ajmg.a.62856
    By:
    • Khan, Atta Ullah;
    • Khan, Ibrar;
    • Khan, Muhammad Ismail;
    • Latif, Muhammad;
    • Siddiqui, Muhammad Imran;
    • Khan, Shafi Ullah;
    • Htar, Thet Thet;
    • Wahid, Ghazala;
    • Ullah, Ikram;
    • Bibi, Fehmida;
    • Khan, Asifullah;
    • Naseer, Muhammad Imran;
    • Seo, Go Hun;
    • Jelani, Musharraf
    Publication type:
    Article
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