eP262: De novo heterozygous variant in the RAB11B gene presenting with combined cardiac defect and neurodevelopmental disorder: A case report

Abstract

Open access

Peer reviewed

Moon Ley Tung, Shelby Romoser, Jaclyn Kotlarek, Taylor Warner, Amy Calhoun and Nicole Safina

Genetics in medicine, Vol.24(3), pp.S166-S166

03/2022

DOI: 10.1016/j.gim.2022.01.297

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Title: Subtitle: eP262: De novo heterozygous variant in the RAB11B gene presenting with combined cardiac defect and neurodevelopmental disorder: A case report
Creators: Moon Ley Tung - University of Iowa
Shelby Romoser - University of Iowa
Jaclyn Kotlarek - University of Iowa
Taylor Warner - University of Iowa
Amy Calhoun - Stead Family Department of Pediatrics, Division of Medical Genetics and Genomics, University of Iowa
Nicole Safina - University of Iowa
Resource Type: Abstract
Publication Details: Genetics in medicine, Vol.24(3), pp.S166-S166
Publisher: Elsevier Inc
DOI: 10.1016/j.gim.2022.01.297
ISSN: 1098-3600
eISSN: 1530-0366
Language: English
Date published: 03/2022
Academic Unit: Stead Family Department of Pediatrics; Medical Genetics and Genomics
Record Identifier: 9984354498302771

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