Ataxia-telangiectasia with a novel ATM gene mutation and Burkitt leukemia: A case report

Ataxia-telangiectasia (A-T) is an infrequent autosomal recessive disorder that involves multiple systems and is characterized by progressive cerebellar ataxia, oculocutaneous telangiectasias, radiosensitivity, immune deficiency with recurrent respiratory infections, and a tendency to develop lymphoi...

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Detalles Bibliográficos
Autores principales: Ye, Fanghua, Chai, Wenwen, Yang, Minghua, Xie, Min, Yang, Liangchun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2018
Materias:
Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6200993/
https://www.ncbi.nlm.nih.gov/pubmed/30402232
http://dx.doi.org/10.3892/mco.2018.1721

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6200993/
https://www.ncbi.nlm.nih.gov/pubmed/30402232
http://dx.doi.org/10.3892/mco.2018.1721

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