CACNA1A-p.Thr501Met mutation associated with familial hemiplegic migraine: a family report
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Background and aims: Hemiplegic migraine (HM) is a rare form of migraine characterized by the presence of a motor and other types of aura. HM can be sporadic or familial. Familial hemiplegic migraine (FHM) is an autosomal dominan... ...
