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In Vivo Functional Study of Disease-associated Rare Human Variants Using Drosophila
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Dominant and recessive SLC12A2-syndrome
Alisdair McNeill1,2, Paul Aurora3, Kaukab Rajput3
1Department of Neuroscience, The University of Sheffield, Sheffield, UK.
American Journal of Medical Genetics. Part A
|November 19, 2021
Summary
No abstract available in PubMed .
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