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Autor:
Hollander, B. den, Veenvliet, A.R.J., Lindenschot, M., Essen, P. van, Peters, G., Santos-Gómez, A., Olivella, M., Altafaj, X., Brands, M.M., Jacobs, B.A.W., Karnebeek, C.D. van
Publikováno v:
Molecular Genetics and Metabolism, 138, 3
Molecular Genetics and Metabolism, 138
Molecular Genetics and Metabolism, 138, 107523
Molecular Genetics and Metabolism, 138
Molecular Genetics and Metabolism, 138, 107523
Item does not contain fulltext RATIONALE: To date, causal therapy is potentially available for GRIN2B-related neurodevelopmental disorder (NDD) due to loss-of-function (LoF) variants in GRIN2B, resulting in dysfunction of the GluN2B subunit-containin