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However, in the case of dominant-negative mutations, where the mutant protein can interfere with the function of a protein translated from the unaffected allele, this approach may not prove successful, although such examples are considered rare in epilepsy (Orhan et al., 2014)
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Although large multicenter trials in BPPV/Ménière’s are lacking, the low risk profile of B12 and its foundational neurological roles make it a compelling adjunct
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