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

Joanne Trinh; Irina Hüning; Nadja Budler; Volker Hingst; Katja Lohmann; Gabriele Gillessen-Kaesbach

doi:10.1038/jhg.2017.73

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

Joanne Trinh, Irina Hüning, Nadja Budler, Volker Hingst, Katja Lohmann, Gabriele Gillessen-Kaesbach

University of Rostock

Original language	English
Journal	Journal of Human Genetics
Volume	62
Issue number	11
Pages (from-to)	1005-1006
Number of pages	2
ISSN	1434-5161
DOIs	https://doi.org/10.1038/jhg.2017.73
Publication status	Published - 01.11.2017

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This output contributes to the following UN Sustainable Development Goals (SDGs)

SDG 3 Good Health and Well-being

Research Areas and Centers

Research Area: Medical Genetics

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10.1038/jhg.2017.73

Cite this

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title = "A novel de novo mutation in CSNK2A1: Reinforcing the link to neurodevelopmental abnormalities and dysmorphic features",

author = "Joanne Trinh and Irina H{\"u}ning and Nadja Budler and Volker Hingst and Katja Lohmann and Gabriele Gillessen-Kaesbach",

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AU - Trinh, Joanne

AU - Hüning, Irina

AU - Budler, Nadja

AU - Hingst, Volker

AU - Lohmann, Katja

AU - Gillessen-Kaesbach, Gabriele

PY - 2017/11/1

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M3 - Letters

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JF - Journal of Human Genetics

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

UN SDGs

Research Areas and Centers

Access to Document

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