MOLECULAR BASES OF DOMINANT ATAXIAS: EPISODIC ATAXIA 2, SPINOCEREBELLAR ATAXIA 6 AND THE ROLE OF CACNA1A GENE MUTATIONS
- 2 Anni 1999/2001
- 82.633€ Totale Fondi
Descrizione non disponibile
Pubblicazioni Scientifiche
- AMERICAN JOURNAL OF HUMAN GENETICS
Complete loss of P/Q calcium channel activity caused by a CACNA1A missense mutation carried by patients with episodic ataxia type 2
- BRAIN RESEARCH BULLETIN
Spinocerebellar ataxia type 6: Channelopathy or glutamine repeat disorder?
- CYTOGENETIC AND GENOME RESEARCH
Spinocerebellar ataxia type 6 and episodic ataxia type 2: differences and similarities between two allelic disorders
- GENE
A fine physical map of the CACNA1A gene region on 19p13.1-p13.2 chromosome
- NEURON
A Cacna1a knockin migraine mouse model with increased susceptibility to cortical spreading depression
