Detection and quantification of a KIF11 mosaicism in a subject presenting familial exudative vitreoretinopathy with microcephaly

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Title:	Detection and quantification of a KIF11 mosaicism in a subject presenting familial exudative vitreoretinopathy with microcephaly
Author(s):	Karjosukarso, D.W.; Cremers, F.P.M. ; Nouhuys, C.E. van; Collin, R.W.J.
Publication year:	2018
Source:	European Journal of Human Genetics, vol. 26, iss. 12, (2018), pp. 1819-1823
ISSN:	1018-4813
DOI:	https://doi.org/10.1038/s41431-018-0243-y
Publication type:	Article / Letter to editor
Please use this identifier to cite or link to this item : http://hdl.handle.net/2066/198268
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Subject:	All institutes and research themes of the Radboud University Medical Center Radboudumc 12: Sensory disorders DCMN: Donders Center for Medical Neuroscience
Organization:	Human Genetics
Journal title:	European Journal of Human Genetics
Volume:	vol. 26
Issue:	iss. 12
Page start:	p. 1819
Page end:	p. 1823