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Dominant‐negative effects of KCNQ2 mutations are associated with epileptic encephalopathy

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Year: 2013
Type: article
Source: Annals of Neurology
DOI: 10.1002/ana.24080
Authors: Gökce Orhan, Merle Bock, Dorien Schepers, Elena I. Ilina, Stephanie Nadine Reichel, Heidi Löffler, Nicole Jezutkovic, Sarah Weckhuysen, Simone Mandelstam, Arvid Suls, Timm Danker, Elke Guenther, Ingrid E. Scheffer, Peter De Jonghe, Holger Lerche, Snezana Maljevic
Institutions: Hertie Institute for Clinical Brain Research, University of Tübingen, VIB-UAntwerp Center for Molecular Neurology, University of Antwerp, Kempenhaeghe, Institute Born-Bunge, The University of Melbourne, Florey Institute of Neuroscience and Mental Health, Royal Children's Hospital, Austin Hospital, Austin Health, Antwerp University Hospital
Language: English

Topic: Ion channel regulation and function
Subfield: Molecular Biology
Field: Biochemistry, Genetics and Molecular Biology
Domain: Life Sciences
SDG: Good health and well-being

Open Access status: closed

Funders: European Science Foundation, Bundesministerium für Bildung und Forschung, National Institutes of Health
Awards: G1021263441, G1084786122, G2927624783, G4312656367, G6571049222
OpenAlex ID: W1892287811
FWCI: 6.553
Cites: 32
Cited by: 285
Related to: 10
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