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Authors
Fathi, Nazanin
Nirouei, Matineh
Salimian Rizi, Zahra
Fekrvand, Saba
Abolhassani, Hassan
Salami, Fereshte
Ketabforoush, Arsh Haj Mohamad Ebrahim
Azizi, Gholamreza
Saghazadeh, Amene
Esmaeili, Marzie
Almasi-Hashiani, Amir
Rezaei, Nima
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Funding
Funding for this research was provided by:
Tehran University of Medical Sciences and Health Services (59130)
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Article History
Received: 22 November 2023
Accepted: 30 June 2024
First Online: 11 July 2024
Change Date: 9 August 2024
Change Type: Update
Change Details: The original version of this paper was updated due to typographical errors found in the body text.
Declarations
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: Understanding the interplay between genotype and phenotype in patients with NF-kB1 and NF-kB2 defects is crucial for refining diagnostic strategies and developing potentially more effective treatment approaches, possibly advancing age-related disease progression predictions.
: The authors declare no competing interests.
