A Recurrent De Novo PACS2 Heterozygous Missense Variant Causes Neonatal-Onset Developmental Epileptic Encephalopathy, Facial Dysmorphism, and Cerebellar Dysgenesis (vol 102, pg 995, 2018)

DDD Study, C4RCD Res Grp

Research output: Contribution to journalErratum / corrigendum / retractionsAcademic

4 Citations (Web of Science)
Original languageEnglish
Pages (from-to)631-631
Number of pages1
JournalAmerican Journal of Human Genetics
Issue number4
Publication statusPublished - 4 Oct 2018

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