Identification of a de novo variant in CHUK in a patient with an EEC/AEC syndrome-like phenotype and hypogammaglobulinemia

Khandelwal, K.D.; Ockeloen, C.W.; Venselaar, H.; Boulanger, C.; Brichard, B.; Sokal, E.; Pfundt, R.; Rinne, T.; van Beusekom, E.; Bloemen, M.; Vriend, G.; Revencu, N.; Carels, C.E.L; van Bokhoven, H.; Zhou, H.

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2017

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American Journal of Medical Genetics. Part A, 173, 7, (2017), pp. 1813-1820

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1552-4825

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https://doi.org/10.1002/ajmg.a.38274

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Article / Letter to editor

Please use this identifier to cite or link to this item: https://hdl.handle.net/2066/177771

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Identification of a de novo variant in CHUK in a patient with an EEC/AEC syndrome-like phenotype and hypogammaglobulinemia

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