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A novel mechanism for variable phenotypic expressivity in Mendelian diseases uncovered by an AU-rich element (ARE)-creating mutation

Crossref DOI link: https://doi.org/10.1186/s13059-017-1274-3

Published Online: 2017-07-28

Published Print: 2017-12

Update policy: https://doi.org/10.1007/springer_crossmark_policy

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