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by Møller, R.S. et al.
Wilhelm Johannsen Centre for Functional Genome Research, Institute of Cellular and Molecular Medicine, University of Copenhagen, Blegdamsvej 3, Denmark

In the present study, we show that truncating mutations of DYRK1A result in a clinical phenotype including microcephaly.
Am. J. Hum. Genet. 2008; 5:1165-70

[See paper]

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