ADAT3-related neurodevelopmental disorder in 24 new patients with a high frequency of the p.Val144Met and a new founder variant.
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- Scientific Reports, 2025, v. 15, n. 1, p. 1, doi. 10.1038/s41598-025-06857-2
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- Article
Works matching AU Abdel-Aleem, Asmaa F.
Results: 2
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A Novel Truncating Mutation in PAX1 Gene Causes Otofaciocervical Syndrome Without Immunodeficiency.
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- Journal of Molecular Neuroscience, 2023, v. 73, n. 11/12, p. 976, doi. 10.1007/s12031-023-02170-7
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- Article