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See Latest ArticlesDe novo STXBP1 mutations in mental retardation and nonsyndromic epilepsy
Annals of Neurology , 06/29/09
Hamdan FF et al. - The results suggest that STXBP1 disruption is associated with autosomal dominant mental retardation and nonsyndromic epilepsy.
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Urate as a Predictor of the Rate of Clinical Decline in Parkinson Disease
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Today in Seizure...keeping you current
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