Autor:	Lorenzo, Verriello, Giada, Pauletto, Annacarmen, Nilo, Incoronata, Lonigro, Elena, Betto, Mariarosaria, Valente, Francesco, Curcio, Gian Luigi, Gigli
Rok vydání:	2021
Předmět:	Epilepsy Cerebellar Ataxia Humans Ataxia Nystagmus Pathologic
Zdroj:	Journal of neurology. 268(11)
ISSN:	1432-1459
Popis:	Episodic ataxia type 2 (EA2) is a hereditary disorder characterized by paroxysmal attacks of ataxia, vertigo and nausea, due to mutations in the CACNA1A gene, which encodes for α1 subunit of the P/Q-type voltage-gated Ca
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=pmid________::4db3e87b8d934ed9647016f661d623ea https://pubmed.ncbi.nlm.nih.gov/33983550 Zobrazit plný text záznamu Full text from SpringerLink