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
ISSN1530-6860
AutoresColin 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
ResumoSPECIFIC 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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