Suchergebnisse - CACNA1G

1

Preparation and Functional Identification of a Novel Conotoxin QcMNCL-XIII0.1 from

von: Han Zhang

2022, in: Toxins

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2

Zonisamide can ameliorate the voltage-dependence alteration of the T-type calcium channel CaV3.1 caused by a mutation responsible for spinocerebellar ataxia

von: Naoyuki Hara

2020, in: Molecular Brain

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3

Ataxic phenotype with altered Ca

von: Hashiguchi, Shunta

2019, in: Neurobiology of disease

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4

Ataxic phenotype with altered CaV3.1 channel property in a mouse model for spinocerebellar ataxia 42

von: Shunta Hashiguchi

2019, in: Neurobiology of Disease

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5

Genetic paroxysmal neurological disorders featuring episodic ataxia and epilepsy (Amadori E et al., 2022)

von: Gazulla, José

2022, in: Edge minimization in de Bruijn graphs

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6

A clinical survey of mosaic single nucleotide variants in disease-causing genes detected by exome sequencing

von: Ye Cao

2019, in: Genome Medicine

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7

Episodic Vestibulocerebellar Ataxia Associated with a CACNA1G Missense Variant

von: José Gazulla

2021, in: Case Reports in Neurology

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8

Regulation of gene expression by 17β-estradiol in the arcuate nucleus of the mouse through ERE-dependent and ERE-independent mechanisms

von: Yang, Jennifer A.

2016, in: Childhood-only epilepsy with generalized tonic-clonic seizures: A well-defined epileptic syndrome

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