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Case Reports

. 2017 Nov;62(11):1005-1006.

doi: 10.1038/jhg.2017.73. Epub 2017 Jul 20.

A novel de novo mutation in CSNK2A1: reinforcing the link to neurodevelopmental abnormalities and dysmorphic features

Joanne Trinh¹, Irina Hüning², Nadja Budler², Volker Hingst³, Katja Lohmann¹, Gabriele Gillessen-Kaesbach²

Affiliations

Affiliations

¹ Institute of Neurogenetics, University of Lübeck, Lübeck, Germany.
² Institut für Humangenetik, Universität zu Lübeck, Lübeck, Germany.
³ Institut für Diagnostische und Interventionelle Radiologie, Universitätsmedizin Rostock, Rostock, Germany.

PMID: 28725024
DOI: 10.1038/jhg.2017.73

Case Reports

A novel de novo mutation in CSNK2A1: reinforcing the link to neurodevelopmental abnormalities and dysmorphic features

Joanne Trinh et al. J Hum Genet. 2017 Nov.

. 2017 Nov;62(11):1005-1006.

doi: 10.1038/jhg.2017.73. Epub 2017 Jul 20.

Authors

Joanne Trinh¹, Irina Hüning², Nadja Budler², Volker Hingst³, Katja Lohmann¹, Gabriele Gillessen-Kaesbach²

Affiliations

¹ Institute of Neurogenetics, University of Lübeck, Lübeck, Germany.
² Institut für Humangenetik, Universität zu Lübeck, Lübeck, Germany.
³ Institut für Diagnostische und Interventionelle Radiologie, Universitätsmedizin Rostock, Rostock, Germany.

PMID: 28725024
DOI: 10.1038/jhg.2017.73

No abstract available

PubMed Disclaimer

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