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

Bi, X., Mulhern, M. S., Spiegel, E., Wapner, R. J., Levy, B., Bain, J. M., & Liao, J. (2023). 3′ UTR Deletion of FBXO28 in a Patient with Brain Abnormalities and Developmental Delay. Genes, 14(9), 1687. https://doi.org/10.3390/genes14091687
Authors:
Xin Bi
Maureen S. Mulhern
Erica Spiegel
Ronald J. Wapner
Brynn Levy
Jennifer M. Bain
Jun Liao
Affiliated Authors:
Xin Bi
Maureen S. Mulhern
Erica Spiegel
Ronald J. Wapner
Brynn Levy
Jennifer M. Bain
Jun Liao
Columbia Affiliation:
Subjects:
Genomic Rearrangements and Copy Number Variations (OpenAlex Topic)
Standards and Guidelines for Genetic Variant Interpretation (OpenAlex Topic)
Molecular Basis of Rett Syndrome and Related Disorders (OpenAlex Topic)
Brain Diseases (MeSH)
Intellectual Disability (MeSH)
Nervous System Malformations (MeSH)
Author Keywords:
3′ utr deletion
brain abnormalities
chromosome 1q42.11 region
developmental delay
fbxo28
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Publication Type:
Article
Unique ID:
10.3390/genes14091687
PMID:
37761828
DOI:
10.3390/genes14091687
Journal:
Genes
Publication Date:
Data Source:
Scopus
Source Link:
View Scopus Record
View OpenAlex Record

Record Created: