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Updated: Dec 15, 2025

In Vivo Functional Study of Disease-associated Rare Human Variants Using Drosophila
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Correction: SMAD6 variants in craniosynostosis: genotype and phenotype evaluation

Eduardo Calpena1, Araceli Cuellar2, Krithi Bala2

  • 1MRCWeatherall Institute of MolecularMedicine, University of Oxford, John Radcliffe Hospital, Oxford, UK.

Genetics in Medicine : Official Journal of the American College of Medical Genetics
|July 9, 2020
PubMed
Summary

This study has published an amendment. Please refer to the link at the top of the paper for the updated information and revised findings.

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