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Title:           Common Variable Immunodeficiency and Neurodevelopmental Delay Due to a 13Mb Deletion on Chromosome 4 Including the NFKB1 Gene: A Case Report
Subject:         Syndromic immunodeficiencies are a heterogeneous group of inborn errors of immunity that can affect the development of non-immune organs and systems
Keywords:        primary immunodeficiencies, syndromic immunodeficiencies, common variable immunodeficiency, nfkb1, chromosomal rearrangements
Author:          Clara Franco-Jarava
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      Title: Common Variable Immunodeficiency and Neurodevelopmental Delay Due to a 13Mb Deletion on Chromosome 4 Including the NFKB1 Gene: A Case Report
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        Title: Introduction
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       Item: 
        Title: Case Description
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       Item: 
        Title: Extended Immunological Characterization of the Patient
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       Item: 
        Title: Identification of a Large Deletion in Chromosome 4 Affecting 53 Genes
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       Item: 
        Title: aCGH Reanalysis Revealed NFKB1 Haploinsufficiency Underlying the CVID Phenotype
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        Title: Discussion
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        Title: Data Availability Statement
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       Item: 
        Title: Ethics Statement
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       Item: 
        Title: Author Contributions
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       Item: 
        Title: Funding
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       Item: 
        Title: Supplementary Material
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       Item: 
        Title: References
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    Title: Common Variable Immunodeficiency and Neurodevelopmental Delay Due to a 13Mb Deletion on Chromosome 4 Including the NFKB1 Gene: A Case Report
    Author: Clara Franco-Jarava
    Subject: Syndromic immunodeficiencies are a heterogeneous group of inborn errors of immunity that can affect the development of non-immune organs and systems
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  Checksum: f9c8cbbe
   Type: CRC32
  Checksum: df3f5c6bd3ffaf80339e27e98ac9b8f4
   Type: MD5
  Checksum: e02fbe5cc4ee42f6e4398539f4ee325586d0814c
   Type: SHA-1
  Checksum: 138ec614b148e3b4d617bbf9768f5a9efe16c09b498a2e8fd383079e1f3cca39
   Type: SHA-256