ATP1A3 Mutations Implicated in Another Rare Disease

ATP1A3 Mutations Implicated in Another Rare Disease

Mutations in ATP1A3 are responsible for yet another disease: CAPOS syndrome as reported in the Orphanet Journal of Rare Diseases. A collaborative team of researchers from Canada & UK made the discovery. The more discoveries like these, the broader the research interest will be in ATP1A3 and the more likely we’ll make leaps and bounds toward a cure. http://www.ojrd.com/content/pdf/1750-1172-9-15.pdf.

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