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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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| Publicado no: | Mol Clin Oncol |
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| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
D.A. Spandidos
2018
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6200993/ https://ncbi.nlm.nih.gov/pubmed/30402232 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3892/mco.2018.1721 |
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