Elevated IgM levels as a marker for a unique phenotype in patients with Ataxia telangiectasia
Abstract 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 s...
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Format: | Book |
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BMC,
2018-06-01T00:00:00Z.
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A1234.567 |
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