Related Experiment Video
Updated: Jun 3, 2025

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In Vivo Functional Study of Disease-associated Rare Human Variants Using Drosophila
Published on: August 20, 2019
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Extreme Phenotypic Variation in Siblings with Identical Homozygous Mutations Causing ADA2 Deficiency: A Case Series
Muhammed D Aksu1,2, Seza Özen3, Tekin Aksu4
1Hacettepe University Faculty of Medicine, Ankara, Türkiye
Summary
No abstract available in PubMed .
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