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Héctor Anta

Spanish National Research Council

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CPEB alteration and aberrant transcriptome-polyadenylation lead to a treatable SLC19A3 deficiency in Huntington's disease.

2021 Science Translational Medicine
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I03 CPEB alteration and aberrant transcriptome-polyadenylation unveil a treatable vitamin B1 deficiency in huntington’s disease

2021 Journal of Neurology, Neurosurgery, and Psychiatry
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