Showing 1 - 2 results of 2 for search 'Raja Hussain Ali', query time: 0.01s Refine Results
  1. 1
    A novel Homozygous Mutation in SPTBN4 (Spectrin beta chain, non-erythrocytic 4) with syndromic neurodevelopmental phenotype in a consanguineous family of Saudi Origin.

    A novel Homozygous Mutation in SPTBN4 (Spectrin beta chain, non-erythrocytic 4) with syndromic neurodevelopmental phenotype in a consanguineous family of Saudi Origin. by Raja Hussain Ali, Muhammad Umair

    Published 2024-02-01
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  2. 2
    Deciphering a Novel TTI2 Mutation in a Saudi Proband with IDDAR39: A Clinical and Genetic Study

    Deciphering a Novel TTI2 Mutation in a Saudi Proband with IDDAR39: A Clinical and Genetic Study by Muhammad Umair, Saleh Althenayyan, Raja Hussain Ali

    Published 2024-02-01
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