Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the P/Q-type calcium channel alfa 1-subunit gene (CACNL1A4) on chromosome 19p13.1
Academic Article
Publication Date:
1996
Iris type:
1.1 Articolo in rivista
List of contributors:
Ophoff, R. A.; Terwindt, G. M.; Vergouwel, M. N.; VAN EIJK, R.; Oefner, P. J.; Hoffman, S. M. G.; Lamerdin, J. E.; Mohrenweiser, H. W.; Bulman, D. E.; Ferrari, Maurizio; Haan, J.; Frants, R. R.
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