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

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Publication year
2017
Author(s)
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.
Source
American Journal of Medical Genetics. Part A, 173, 7, (2017), pp. 1813-1820
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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/2066/177771   https://hdl.handle.net/2066/177771
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