CC2D1A causes ciliopathy, intellectual disability, heterotaxy, renal dysplasia, and abnormal CSF flow

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dc.contributor.authorKim, Angelina Haesoo
dc.contributor.authorSakin, Irmak
dc.contributor.authorViviano, Stephen
dc.contributor.authorTuncel, Gulten
dc.contributor.authorAguilera, Stephanie Marie
dc.contributor.authorGoles, Gizem
dc.contributor.authorJeffries, Lauren
dc.contributor.authorJi, Weizhen
dc.contributor.authorLakhani, Saquib A.
dc.contributor.authorKose, Canan Ceylan
dc.contributor.authorSilan, Fatma
dc.contributor.authorOner, Sukru Sadik
dc.contributor.authorKaplan, I, Oktay
dc.contributor.authorErgoren, Mahmut Cerkez
dc.contributor.authorMishra\\-Gorur, Ketu
dc.contributor.authorGunel, Murat
dc.contributor.authorSag, Sebnem Ozemri
dc.contributor.authorTemel, Sehime G.
dc.contributor.authorDeniz, Engin
dc.contributor.authorMarmaRare Grp
dc.date.accessioned2025-10-16T15:12:50Z
dc.date.issued2024
dc.identifier.doi10.26508/lsa.202402708
dc.identifier.otherWOS:001458798700001
dc.identifier.urihttps://openaccess.acibadem.edu.tr/handle/11443/5631
dc.publisherLIFE SCIENCE ALLIANCE LLC
dc.sourceLIFE SCIENCE ALLIANCE
dc.titleCC2D1A causes ciliopathy, intellectual disability, heterotaxy, renal dysplasia, and abnormal CSF flow
dc.typeArticle

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