Πλοήγηση ανά Θέμα "A53T mutation"
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A Swedish family with de novo alpha-synuclein A53T mutation: Evidence for early cortical dysfunction
(2009)A de novo alpha-symaclein A53T (p.Ala53 Th; c.209G > A) mutation has been identified in a Swedish family with autosomal dominant Parkinson's disease (PD). Two affected individuals had early-onset (before 31 and 40 years), ...