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Updated: Nov 6, 2025

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In Vivo Functional Study of Disease-associated Rare Human Variants Using Drosophila
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Two novel bi-allelic KDELR2 missense variants cause osteogenesis imperfecta with neurodevelopmental features
Stephanie Efthymiou1, Isabella Herman2,3,4, Fatima Rahman5
1Department of Neuromuscular Disorders, Queen Square Institute of Neurology, University College London, London, UK.
American Journal of Medical Genetics. Part A
|May 8, 2021
Abstract
No abstract available in PubMed .
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