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4 novel missense mutations identified in ataxia patients http://t.co/FnclIpCFCM #OJRD #RareDisease
Phenotype and frequency of STUB1 mutations: next-generation screenings in Caucasian ataxia and spastic paraplegia cohorts
Overview of attention for article published in Orphanet Journal of Rare Diseases, April 2014
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Good Attention Score compared to outputs of the same age (67th percentile)
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Above-average Attention Score compared to outputs of the same age and source (55th percentile)
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