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Post by Thomas Way on Aug 4, 2012 1:41:00 GMT -5
Researchers in the states have found a gene mutation (ATP1A3) that exists in around 70% of AHC sufferers.
This is great news. Now that the scientists understand what processes cause the condition they can start working on finding an effective treatment or even a cure.
There's more info at the Alternating Hemiplegia foundation: ahckids.org
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