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bcl10 protein, human
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Genetic Markers
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Lymphoma (4 types) and B-cell purified subpopulation gene expression profiling
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BCL10 Deficiency Presenting as Severe Combined Immunodeficiency Escaping Newborn Screening.
Inherited Human BCL10 Deficiencies.
BCL10 loss-of-function novel mutation leading to atypical severe combined immunodeficiency.
BCL10 correlates with bad prognosis and immune infiltration of tumor microenvironment in hepatocellu…
BCL10 Mutants: Architects of Oncogenic Signaling Provide a Blueprint for Precision Medicine.
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Genetics of the Early and Late Response to Allergen Challenge
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