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Identification of De Novo DNMT3A Mutations That Cause West Syndrome by Using Whole-Exome Sequencing

Crossref DOI link: https://doi.org/10.1007/s12035-017-0483-9

Published Online: 2017-04-06

Published Print: 2018-03

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

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