A novel recurrent mutation in ATP1A3 causes CAPOS syndrome

Overview of attention for article published in Orphanet Journal of Rare Diseases, January 2014

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In the top 25% of all research outputs scored by Altmetric
High Attention Score compared to outputs of the same age (85th percentile)
High Attention Score compared to outputs of the same age and source (80th percentile)

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RT @clambert112358: Case 2: CAPOS syndrome due to ATP1A3 gene mutation https://t.co/P2QCKAYshU #MDSCongress2017

RT @clambert112358: Case 2: CAPOS syndrome due to ATP1A3 gene mutation https://t.co/P2QCKAYshU #MDSCongress2017

Case 2: CAPOS syndrome due to ATP1A3 gene mutation https://t.co/P2QCKAYshU #MDSCongress2017

http://t.co/58dXPCAWjb ATP1A3 Mutations cause another disease- CAPOS. Collabortive UK/CA team reports. New clues 4 cure #raredisease

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