De Novo Variants Disturbing the Transactivation Capacity of POU3F3 Cause a Characteristic Neurodevelopmental Disorder

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Publication year
2019
Author(s)
Snijders Blok, L.
Kleefstra, T.
Venselaar, H.
Maas, Saskia
Kroes, Hester Y.
Lachmeijer, Augusta M. A.
Gilissen, C.
Pfundt, R.P.
Brunner, H.G.
Fisher, S.E.
Source
American Journal of Human Genetics, 105, 2, (2019), pp. 403-412
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Publication type
Article / Letter to editor
Please use this identifier to cite or link to this item: https://hdl.handle.net/2066/206058   https://hdl.handle.net/2066/206058
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