De novo and bi-allelic variants in AP1G1 cause neurodevelopmental disorder with developmental delay, intellectual disability, and epilepsy

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Publication year
2021
Author(s)
Usmani, M.A.
Ahmed, Z.M.
Magini, P.
Pienkowski, V.M.
Rasmussen, K.
Hernan, R.
Rasheed, F.
Bokhoven, H. van
Riazuddin, Sheikh
Riazuddin, Saima
Source
American Journal of Human Genetics, 108, 7, (2021), pp. 1330-1341
ISSN
DOI
Publication type
Article / Letter to editor
Please use this identifier to cite or link to this item: https://hdl.handle.net/2066/235087   https://hdl.handle.net/2066/235087
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