Dystonia and cerebellar atrophy in Cacna1a null mice lacking P/Q calcium channel activity

Autor:	Fletcher, Cf, Tottene, A, Lennon, Va, Wilson, Sm, Dubel, Sj, Paylor, R, Hosford, Da, Tessarollo, L, Mcenery, Mw, Pietrobon, Daniela, Copeland, Ng, Jenkins, Na
Rok vydání:	2001
Předmět:	congenital hereditary and neonatal diseases and abnormalities medicine.medical_specialty Cerebellum Ataxia Patch-Clamp Techniques Cerebellar Ataxia Mice Transgenic Biochemistry Cav2.1 omega-Conotoxins Calcium Channels Q-Type Mice Calcium Channels N-Type omega-Conotoxin GVIA Internal medicine Genetics medicine Animals Humans Molecular Biology Cells Cultured Episodic ataxia Dystonia biology business.industry Calcium channel Calcium Channels P-Type medicine.disease Calcium Channel Blockers Endocrinology medicine.anatomical_structure Migraine Gene Targeting biology.protein Cerebellar atrophy Nimodipine Calcium Channels medicine.symptom business Biotechnology
Popis:	SPECIFIC AIMSP/Q-type voltage-dependent calcium channel CACNA1A mutations cause dominantly inherited migraine, episodic ataxia, and cerebellar atrophy in humans and recessively inherited ataxia, ep...
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fa622d77c29eeb05aa3bc4be4854c196 http://hdl.handle.net/11577/1481532 Zobrazit plný text záznamu