3' UTR Deletion of FBXO28 in a Patient with Brain Abnormalities and Developmental Delay.

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Bibliographic Details
Title: 3' UTR Deletion of FBXO28 in a Patient with Brain Abnormalities and Developmental Delay.
Authors: Bi X; Department of Pathology and Cell Biology, Columbia University Irving Medical Center, New York, NY 10032, USA., Mulhern MS; Department of Pathology and Cell Biology, Columbia University Irving Medical Center, New York, NY 10032, USA.; Department of Neurology, Columbia University Irving Medical Center, New York, NY 10032, USA., Spiegel E; Department of Obstetrics and Gynecology, Columbia University Irving Medical Center, New York, NY 10032, USA., Wapner RJ; Department of Obstetrics and Gynecology, Columbia University Irving Medical Center, New York, NY 10032, USA., Levy B; Department of Pathology and Cell Biology, Columbia University Irving Medical Center, New York, NY 10032, USA., Bain JM; Department of Neurology, Columbia University Irving Medical Center, New York, NY 10032, USA.; Department of Pediatrics, Columbia University Irving Medical Center, New York, NY 10032, USA., Liao J; Department of Pathology and Cell Biology, Columbia University Irving Medical Center, New York, NY 10032, USA.
Source: Genes [Genes (Basel)] 2023 Aug 25; Vol. 14 (9). Date of Electronic Publication: 2023 Aug 25.
Publication Type: Case Reports; Journal Article
Journal Info: Publisher: MDPI Country of Publication: Switzerland NLM ID: 101551097 Publication Model: Electronic Cited Medium: Internet ISSN: 2073-4425 (Electronic) Linking ISSN: 20734425 NLM ISO Abbreviation: Genes (Basel) Subsets: MEDLINE
Database: MEDLINE Ultimate
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ISSN:2073-4425
DOI:10.3390/genes14091687