CFAP99 deficiency leads to heterotaxy and scoliosis

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dc.contributor.authorAy, Beril
dc.contributor.authorViviano, Stephen
dc.contributor.authorDogan, Ozlem Akgun
dc.contributor.authorAlanay, Yasemin
dc.contributor.authorDeniz, Engin
dc.date.accessioned2025-10-16T15:12:20Z
dc.date.issued2024
dc.description.abstract57th Conference of the European-Society-of-Human-Genetics (ESHG), Berlin, GERMANY, JUN 01-04, 2024
dc.identifier.otherWOS:001421430503422
dc.identifier.urihttps://openaccess.acibadem.edu.tr/handle/11443/5386
dc.publisherSPRINGERNATURE
dc.sourceEUROPEAN JOURNAL OF HUMAN GENETICS
dc.titleCFAP99 deficiency leads to heterotaxy and scoliosis
dc.typeMeeting Abstract

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