Clustered mutations in the GRIK2 kainate receptor subunit gene underlie diverse neurodevelopmental disorders

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Publisher’s version
Publication year
2021
Author(s)
Stolz, Jacob R.
Foote, K.
Veenstra-Knol, Hermine E.
Pfundt, R.P.
Broeke, Sanne W. ten
Leeuw, N. de
Bon, B.W. van
Carvill, G.L.
Swanson, Geoffrey T.
Source
American Journal of Human Genetics, 108, 9, (2021), pp. 1692-1709
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DOI
Publication type
Article / Letter to editor
If a DOI or any other persistent identifier is unavailable, please use the following repository identifier to link to this item: https://hdl.handle.net/2066/237141   https://hdl.handle.net/2066/237141
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