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Updated: Nov 27, 2025

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In Vivo Functional Study of Disease-associated Rare Human Variants Using Drosophila
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A de novo ATXN2L variant in a child with developmental delay and macrocephaly
Fatema Alzahrani1, Turki H Albatti2, Fowzan S Alkuraya1,3
1Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
American Journal of Medical Genetics. Part A
|December 7, 2020
Abstract
No abstract available in PubMed .
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