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MECP2, a gene associated with Rett syndrome in humans, shows conserved coding regions, independent Alu insertions, and a novel transcript across primate evolution

Crossref DOI link: https://doi.org/10.1186/s12863-015-0240-x

Published Online: 2015-07-07

Published Print: 2015-12

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

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