De novo mutations of SCN1A are responsible for arthrogryposis broadening the SCN1A-related phenotypes

Added 36 days ago (23.10.2021)
Authors: Jaber, D., Gitiaux, C., Blesson, S., Marguet, F., Buard, D., Varela Salgado, M., Kaminska, A., Saada, J., Fallet-Bianco, C., Martinovic, J., Laquerriere, A., Melki, J.
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