A rare case of coronin-1A deficiency with IgM dominant membranoproliferative glomerulonephritis
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Coronin-1A deficiency, caused by mutations in the CORO1A gene, is an autosomal recessive immunodeficiency characterized by T-cell dysfunction and is classified as severe combined immunodeficiency (SCID). This condition presents with lymphopenia, hypogammaglobu... ...
