Seizures, developmental delay, mild intellectual disability, muscular hypotonia, and optic atrophy: About the genetic diagnosis of patient with a novel ATP1A3 mutation

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dc.contributor.authorSaygi, C.
dc.contributor.authorSezerman, U.
dc.date.accessioned2025-10-16T15:22:48Z
dc.date.issued2019
dc.description.abstract52nd Conference of the European-Society-of-Human-Genetics (ESHG), Gothenburg, SWEDEN, JUN 15-18, 2019
dc.identifier.otherWOS:000489313907102
dc.identifier.urihttps://openaccess.acibadem.edu.tr/handle/11443/7887
dc.publisherNATURE PUBLISHING GROUP
dc.sourceEUROPEAN JOURNAL OF HUMAN GENETICS
dc.titleSeizures, developmental delay, mild intellectual disability, muscular hypotonia, and optic atrophy: About the genetic diagnosis of patient with a novel ATP1A3 mutation
dc.typeMeeting Abstract

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