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

Usmani, M.A.; Ahmed, Z.M.; Magini, P.; Pienkowski, V.M.; Rasmussen, K.; Hernan, R.; Rasheed, F.; Bokhoven, H. van; Riazuddin, Sheikh; Riazuddin, Saima

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2021

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American Journal of Human Genetics, 108, 7, (2021), pp. 1330-1341

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0002-9297

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https://doi.orghttps://doi.org/10.1016/j.ajhg.2021.05.007

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Article / Letter to editor

Please use this identifier to cite or link to this item: https://hdl.handle.net/2066/235087

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

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