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PRRT2 gene variant in a child with dysmorphic features, congenital microcephaly, and severe epileptic seizures: genotype-phenotype correlation?

Crossref DOI link: https://doi.org/10.1186/s13052-019-0755-2

Published Online: 2019-12-04

Published Print: 2019-12

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

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