Relevance of biallelic vs monoallelic TNFRSF13B mutations in distinguishing disease-causing from risk-increasing TNFRSF13B variants in antibody deficiency syndromes
Main Authors: | , , , , , , , , , , , , , , , , , , , , , , , , |
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Format: | Conference item |
Published: |
2008
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Summary: |
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