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

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Title:	Identification of a de novo variant in CHUK in a patient with an EEC/AEC syndrome-like phenotype and hypogammaglobulinemia
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.
Publication year:	2017
Source:	American Journal of Medical Genetics. Part A, vol. 173, iss. 7, (2017), pp. 1813-1820
ISSN:	1552-4825
DOI:	http://dx.doi.org/10.1002/ajmg.a.38274
Publication type:	Article / Letter to editor
Please use this identifier to cite or link to this item : http://hdl.handle.net/2066/177771
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Subject:	Molecular Developmental Biology
Organization:	Molecular Developmental Biology
Journal title:	American Journal of Medical Genetics. Part A
Volume:	vol. 173
Issue:	iss. 7
Page start:	p. 1813
Page end:	p. 1820

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