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ArticleJournal of pediatric genetics2021

A Novel c.968C > T homozygous Mutation in the Polynucleotide Kinase 3' - Phosphatase Gene Related to the Syndrome of Microcephaly, Seizures, and Developmental Delay.

Carlos Marcilla Vázquez et al.PubMed ↗Full text ↗Publisher ↗

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