Cargando…
Ataxia Telangiectasia Diagnosed on Newborn Screening–Case Cohort of 5 Years' Experience
Ataxia telangiectasia (AT) is a genetic condition caused by mutations involving ATM (Ataxia Telangiectasia Mutated). This gene is responsible for the expression of a DNA double stranded break repair kinase, the ATM protein kinase. The syndrome encompasses combined immunodeficiency and various degree...
Autores principales: | Mandola, Amarilla B., Reid, Brenda, Sirror, Raga, Brager, Rae, Dent, Peter, Chakroborty, Pranesh, Bulman, Dennis E., Roifman, Chaim M. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6932992/ https://www.ncbi.nlm.nih.gov/pubmed/31921190 http://dx.doi.org/10.3389/fimmu.2019.02940 |
Ejemplares similares
-
Dilemma of Reporting Incidental Findings in Newborn Screening Programs for SCID: Parents’ Perspective on Ataxia Telangiectasia
por: Blom, Maartje, et al.
Publicado: (2019) -
Treatment of Granulomas in Patients With Ataxia Telangiectasia
por: Woelke, Sandra, et al.
Publicado: (2018) -
Newborn Screening for SCID Identifies Patients with Ataxia Telangiectasia
por: Mallott, Jacob, et al.
Publicado: (2012) -
Reconstitution of the Ataxia-Telangiectasia Cellular Phenotype With Lentiviral Vectors
por: Carranza, Diana, et al.
Publicado: (2018) -
Atypical Ataxia Presentation in Variant Ataxia Telangiectasia: Iranian Case-Series and Review of the Literature
por: Moeini Shad, Tannaz, et al.
Publicado: (2022)