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Papers of the Week
A Chinese family with familial hemiplegic migraine type 2 due to a novel missense mutation in ATP1A2.
Abstract
ATP1A2 has been identified as the genetic cause of familial hemiplegic migraine type 2. Over 80 ATP1A2 mutations have been reported, but no data from Chinese family studies has been included. Here, we report the first familial hemiplegic migraine type 2 Chinese family with a novel missense mutation.