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Elevated IgM levels as a marker for a unique phenotype in patients with Ataxia telangiectasia
BACKGROUND: Ataxia telangiectasia (AT) is a rare, multi-systemic, genetic disorder. Mutations in the ATM gene cause dysfunction in cell-cycle, apoptosis and V (D) J recombination leading to neurodegeneration, cellular, humoral immunodeficiencies and predisposition to malignancies. Previous studies h...
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| Publicado no: | BMC Pediatr |
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| Main Authors: | , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2018
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5987459/ https://ncbi.nlm.nih.gov/pubmed/29866155 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12887-018-1156-1 |
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