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Unraveling the genetic complexity of neurodevelopmental disorders: insights from autosomal recessive and de novo variants in a consanguineous family

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dc.contributor.authorSüsgün S.
dc.contributor.authorKesim Y.
dc.contributor.authorSalman B.
dc.contributor.authorYücesan E.
dc.contributor.authorTuncer Kılınç F. N.
dc.contributor.authorÇalık M.
dc.contributor.authorAltıokka Uzun G.
dc.contributor.authorÖzbek U.
dc.contributor.authorUğur İşeri S. A.
dc.date.accessioned2025-07-17T21:50:23Z
dc.date.issued2025-05-24
dc.identifier.citationSüsgün S., Kesim Y., Salman B., Yücesan E., Tuncer Kılınç F. N., Çalık M., Altıokka Uzun G., Özbek U., Uğur İşeri S. A., \"Unraveling the genetic complexity of neurodevelopmental disorders: insights from autosomal recessive and de novo variants in a consanguineous family\", European Human Genetics Conference, Milan, İtalya, 24 - 27 Mayıs 2025, (Özet Bildiri)
dc.identifier.urihttps://hdl.handle.net/20.500.12645/40805
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectSağlık Bilimleri
dc.subjectHealth Sciences
dc.subjectKlinik Tıp (Med)
dc.subjectClinical Medicine (Med)
dc.titleUnraveling the genetic complexity of neurodevelopmental disorders: insights from autosomal recessive and de novo variants in a consanguineous family
dc.typeconferenceObject
dspace.entity.typePublication
local.avesis.id4ff68b58-e90b-4a04-84c2-d4fbc6a1a118

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