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JAGN1 mutation with distinct clinical features; two case reports and literature review
Jagunal homolog 1 (JAGN1) has been recognized as an essential protein in neutrophil function. The mutated JAGN1 is responsible for immunodeficiency related to innate and humoral defense mechanisms. This deficiency impairs neutrophil development and function, leading to recurrent infections and facia...
Autores principales: | Hojabri, Mahsa, Farsi, Yeganeh, Jamee, Mahnaz, Abolhassani, Hassan, Khani, Hedieh Haji Khodaverdi, Karimi, Abdollah, Mesdaghi, Mehrnaz, Chavoshzadeh, Zahra, Sharafian, Samin |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10148515/ https://www.ncbi.nlm.nih.gov/pubmed/37120535 http://dx.doi.org/10.1186/s12887-023-04024-y |
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