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Authors: Nadja Ehmke
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Journal Article
Variants in the SK2 channel gene (KCNN2) lead to dominant neurodevelopmental movement disorders Free
Fanny Mochel and others
Brain, Volume 143, Issue 12, December 2020, Pages 3564–3573, https://doi.org/10.1093/brain/awaa346
Published: 27 November 2020
Journal Article
MN1 C-terminal truncation syndrome is a novel neurodevelopmental and craniofacial disorder with partial rhombencephalosynapsis Free
Christopher C Y Mak and others
Brain, Volume 143, Issue 1, January 2020, Pages 55–68, https://doi.org/10.1093/brain/awz379
Published: 13 December 2019
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