A HOMOZYGOUS TBC1D31 VARIATION AS A POTENTIAL NOVEL CAUSE OF AUTOSOMAL RECESSIVE CONGENITAL ANOMALIES OF THE KIDNEY AND URINARY TRACT

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dc.contributor.authorSaygili, Seha
dc.contributor.authorKosukcu, Can
dc.contributor.authorBastug, Turgut
dc.contributor.authorDogan, Ozlem Akgun
dc.contributor.authorYilmaz, Esra Karabag
dc.contributor.authorUcar, Ayse Kalyoncu
dc.contributor.authorAgbas, Ayse
dc.contributor.authorCanpolat, Nur
dc.contributor.authorCaliskan, Salim
dc.contributor.authorOzaltin, Fatih
dc.date.accessioned2025-10-16T15:14:45Z
dc.date.issued2023
dc.identifier.otherWOS:001091418900078
dc.identifier.urihttps://openaccess.acibadem.edu.tr/handle/11443/6268
dc.publisherSPRINGER
dc.sourcePEDIATRIC NEPHROLOGY
dc.titleA HOMOZYGOUS TBC1D31 VARIATION AS A POTENTIAL NOVEL CAUSE OF AUTOSOMAL RECESSIVE CONGENITAL ANOMALIES OF THE KIDNEY AND URINARY TRACT
dc.typeMeeting Abstract

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