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Tuesday, March 20, 2018

'Missing mutation' found in severe infant epilepsy

http://ift.tt/eA8V8J Researchers have discovered a 'missing mutation' in severe infant epilepsy -- long-suspected genetic changes that might trigger overactive, brain-damaging electrical signaling leading to seizures. They also found early indications that specific anti-seizure medications might prevent disabling brain injury by controlling epilepsy during a crucial period shortly after birth.

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