A de novo missense mutation in synaptotagmin-1 associated with neurodevelopmental disorder desynchronizes neurotransmitter release
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- Extent
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1 Online-Ressource.
- Language
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Englisch
- Bibliographic citation
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A de novo missense mutation in synaptotagmin-1 associated with neurodevelopmental disorder desynchronizes neurotransmitter release ; day:6 ; month:2 ; year:2024 ; pages:1-12
Molecular psychiatry ; (6.2.2024), 1-12
- Creator
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Boven, Maaike A. van
Mestroni, Marta
Zwijnenburg, Petra J. G.
Verhage, Matthijs
Cornelisse, L. Niels
- Contributor
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SpringerLink (Online service)
- DOI
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10.1038/s41380-024-02444-5
- URN
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urn:nbn:de:101:1-2024041511051509424368
- Rights
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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14.08.2025, 10:58 AM CEST
Data provider
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Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Boven, Maaike A. van
- Mestroni, Marta
- Zwijnenburg, Petra J. G.
- Verhage, Matthijs
- Cornelisse, L. Niels
- SpringerLink (Online service)
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Monoallelic de novo AJAP1 loss-of-function variants disrupt trans-synaptic control of neurotransmitter release
Disease relevance of rare VPS13B missense variants for neurodevelopmental Cohen syndrome
Regulation of neurotransmitter release by essential vesicular proteins
The recurrent missense mutation p.(Arg367Trp) in YARS1 causes a distinct neurodevelopmental phenotype
P2 receptor-mediated modulation of neurotransmitter release—an update
Neurotransmitter release and uptake : [proceedings of the NATO Advanced Study Institute "Neurotransmitter Release and Uptake", held at Kuşadası, Turkey, April 19 - 30, 1996]
Epac-mediated modulation of neurotransmitter release from cultured hippocampal neurons
The release of inhibition model reproduces kinetics and plasticity of neurotransmitter release in central synapses
Prediction of Neurodevelopmental Disorders Based on De Novo Coding Variation
The mechanism mediating fast neurotransmitter release at the calyx of Held synapse
Pharmacology of neurotransmitter release
Monitoring neurotransmitter release during behaviour
Monoallelic de novo AJAP1 loss-of-function variants disrupt trans-synaptic control of neurotransmitter release
Disease relevance of rare VPS13B missense variants for neurodevelopmental Cohen syndrome
Regulation of neurotransmitter release by essential vesicular proteins
The recurrent missense mutation p.(Arg367Trp) in YARS1 causes a distinct neurodevelopmental phenotype
P2 receptor-mediated modulation of neurotransmitter release—an update
Neurotransmitter release and uptake : [proceedings of the NATO Advanced Study Institute "Neurotransmitter Release and Uptake", held at Kuşadası, Turkey, April 19 - 30, 1996]
Epac-mediated modulation of neurotransmitter release from cultured hippocampal neurons
The release of inhibition model reproduces kinetics and plasticity of neurotransmitter release in central synapses
Prediction of Neurodevelopmental Disorders Based on De Novo Coding Variation