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 / corrigendumAcademic

Original languageEnglish
Pages (from-to)631-631
Number of pages1
JournalAmerican Journal of Human Genetics
Volume103
Issue number4
DOIs
Publication statusPublished - 4 Oct 2018

Research Output

A Recurrent De Novo PACS2 Heterozygous Missense Variant Causes Neonatal-Onset Developmental Epileptic Encephalopathy, Facial Dysmorphism, and Cerebellar Dysgenesis

Olson, H. E., Jean-Marcais, N., Yang, E., Heron, D., Tatton-Brown, K., van der Zwaag, P. A., Bijlsma, E. K., Krock, B. L., Backer, E., Kamsteeg, E-J., Sinnema, M., Reijnders, M. R. F., Bearden, D., Begtrup, A., Telegrafi, A., Lunsing, R. J., Burglen, L., Lesca, G., Cho, M. T., Smith, L. A. & 31 others, Sheidley, B. R., El Achkar, C. M., Pearl, P. L., Poduri, A., Skraban, C. M., Tarpinian, J., Nesbitt, A. I., van de Putte, D. E. F., Ruivenkamp, C. A. L., Rump, P., Chatron, N., Sabatier, I., De Bellescize, J., Guibaud, L., Sweetser, D. A., Waxler, J. L., Wierenga, K. J., Donadieu, J., Narayanan, V., Ramsey, K. M., Nava, C., Riviere, J-B., Vitobello, A., Mau-Them, F. T., Philippe, C., Bruel, A-L., Duffourd, Y., Thomas, L., Lelieveld, S. H., Brunner, H. G. & DDD Study; C4RCD Res Grp, 3 May 2018, In : American Journal of Human Genetics. 102, 5, p. 995-1007 13 p.

Research output: Contribution to journalArticleAcademicpeer-review

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