New gain-of-function mutation shows CACNA1D as recurrently mutated gene in autism spectrum disorders and epilepsy
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- Alexandra Pinggera
- Department of Pharmacology and Toxicology Center for Molecular Biosciences, University of Innsbruck, 6020 Innsbruck, Austria
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- Luisa Mackenroth
- Institut für Klinische Genetik
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- Andreas Rump
- Institut für Klinische Genetik
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- Jens Schallner
- Abteilung Neuropädiatrie, Medizinische Fakultät Carl Gustav Carus, Technische Universität Dresden, 01307 Dresden, Germany
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- Filippo Beleggia
- Department I of Internal Medicine, University Hospital of Cologne, 50923 Cologne, Germany
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- Bernd Wollnik
- Institute of Human Genetics, University Medical Center Göttingen, 37073 Göttingen, Germany
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- Jörg Striessnig
- Department of Pharmacology and Toxicology Center for Molecular Biosciences, University of Innsbruck, 6020 Innsbruck, Austria
この論文をさがす
収録刊行物
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- Human Molecular Genetics
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Human Molecular Genetics 26 (15), 2923-2932, 2017-05-04
Oxford University Press (OUP)
