Identification of Cytochrome b‐245, beta‐chain gene mutations, and clinical presentations in Iranian patients with X‐linked chronic granulomatous disease

BACKGROUND: X‐linked chronic granulomatous disease (X‐CGD) is an immunodeficiency disorder caused by defects in the gp91(phox) subunit that leads to life‐threatening infections. We aimed to identify CYBB gene mutations and study clinical phenotypes in Iranian patients with probable X‐CGD. METHODS: W...

Descripción completa

Detalles Bibliográficos
Autores principales: Heydari, Atefeh, Abolnezhadian, Farhad, Sadeghi‐Shabestari, Mahnaz, Saberi, Alihossein, Shamsizadeh, Ahmad, Ghadiri, Ata A., Ghandil, Pegah
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Research Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7891530/
https://www.ncbi.nlm.nih.gov/pubmed/33098164
http://dx.doi.org/10.1002/jcla.23637

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7891530/
https://www.ncbi.nlm.nih.gov/pubmed/33098164
http://dx.doi.org/10.1002/jcla.23637

Ejemplares similares