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Whole-exome sequencing identifies a de novo TUBA1A mutation in a patient with sporadic malformations of cortical development: a case report

Crossref DOI link: https://doi.org/10.1186/1756-0500-7-465

Published Online: 2014-07-22

Published Print: 2014-12

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

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