Dure, L.

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De novo loss-of-function KCNMA1 variants are associated with a new multiple malformation syndrome and a broad spectrum of developmental and neurological phenotypes

Liang, L., Li, X., Moutton, S., Schrier Vergano, S. A., Cogné, B., Saint-Martin, A., Hurst, A. C. E., Hu, Y., Bodamer, O., Thevenon, J., et al. (2019) · Human Molecular Genetics

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Treatment approaches for functional neurological disorders in children

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