𝔖 Bobbio Scriptorium
✦   LIBER   ✦

A novel mutation in CACNA1A associated with hemiplegic migraine, cerebellar dysfunction and late-onset cognitive decline

✍ Scribed by T. Freilinger; N. Ackl; A. Ebert; C. Schmidt; B. Rautenstrauss; M. Dichgans; A. Danek


Book ID
119303902
Publisher
Elsevier Science
Year
2011
Tongue
English
Weight
296 KB
Volume
300
Category
Article
ISSN
0022-510X

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


A novel KCNA1 mutation associated with g
✍ Michelle K. Demos; Vincenzo Macri; Kevin Farrell; Tanya N. Nelson; Kristine Chap πŸ“‚ Article πŸ“… 2009 πŸ› John Wiley and Sons 🌐 English βš– 457 KB

## Abstract Episodic Ataxia Type 1 is an autosomal dominant disorder characterized by episodes of ataxia and myokymia. It is associated with mutations in the __KCNA1__ voltage‐gated potassium channel gene. In the present study, we describe a family with novel clinical features including persistent