Neuroimaging features of MOPDII in ten patients with PCNT mutation: A Tertiary Centre Experience

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dc.contributor.authorAkalin, Akcahan
dc.contributor.authorGocmen, Rahsan
dc.contributor.authorSimsek\\-Kiper, Pelin
dc.contributor.authorTaskiran, Ekim
dc.contributor.authorAlanay, Yasemin
dc.contributor.authorHaliloglu, Vildan Goknur
dc.contributor.authorUtine, Gulen Eda
dc.contributor.authorBoduroglu, Koray
dc.date.accessioned2025-10-16T15:13:59Z
dc.date.issued2024
dc.description.abstract56th Annual Conference of the European-Society-of-Human-Genetics (ESHG), Glasgow, SCOTLAND, JUN 10-13, 2023
dc.identifier.otherWOS:001147414902163
dc.identifier.urihttps://openaccess.acibadem.edu.tr/handle/11443/6021
dc.publisherSPRINGERNATURE
dc.sourceEUROPEAN JOURNAL OF HUMAN GENETICS
dc.titleNeuroimaging features of MOPDII in ten patients with PCNT mutation: A Tertiary Centre Experience
dc.typeMeeting Abstract

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