AGM |
AGM-1470 |
myeloid-associated immunoglobulin-like receptor V |
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[agammaglobulinemia 6] This designation has been used for an autosomal recessive primary immunodeficiency characterized by profoundly low or absent serum antibodies and low or absent circulating B-cells due to an early block of B-cell development (Dobbs et al, 2007). The underlying cause is a hypomorphic mutation in the Ig-beta gene, which, in the nomenclature of CD antigens has been given the designation CD79b.
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