Artigo Revisado por pares

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

2001; Wiley; Volume: 15; Issue: 7 Linguagem: Inglês

10.1096/fj.00-0562fje

ISSN

1530-6860

Autores

Colin Fletcher, Angelita Tottene, Vanda A. Lennon, Scott M. Wilson, Stefan Dübel, Richard Paylor, David A. Hosford, Lino Tessarollo, Maureen W. McEnery, Daniela Pietrobon, Neal G. Copeland, Nancy A. Jenkins,

Tópico(s)

Neurological disorders and treatments

Resumo

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...

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