Genetic Risk Variants for Class Switching Recombination Defects in Ataxia-Telangiectasia Patients

BACKGROUND: Ataxia-telangiectasia (A-T) is a rare autosomal recessive disorder caused by mutations in the ataxia telangiectasia mutated (ATM) gene. A-T patients manifest considerable variability in clinical and immunological features, suggesting the presence of genetic modifying factors. A striking...

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Detalles Bibliográficos
Autores principales: Amirifar, Parisa, Mehrmohamadi, Mahya, Ranjouri, Mohammad Reza, Akrami, Seyed Mohammad, Rezaei, Nima, Saberi, Ali, Yazdani, Reza, Abolhassani, Hassan, Aghamohammadi, Asghar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2021
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8821084/
https://www.ncbi.nlm.nih.gov/pubmed/34628594
http://dx.doi.org/10.1007/s10875-021-01147-8

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8821084/
https://www.ncbi.nlm.nih.gov/pubmed/34628594
http://dx.doi.org/10.1007/s10875-021-01147-8

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