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References in periodicals archive ?
HEMPAS erythrocyte band 3 shows a complete absence of poly N-acetyllactosamine.
HEMPAS. Hereditary erythroblastic multinuclearity with positive acidified serum lysis test.
[4] Nonstandard abbreviations: ER, endoplasmic reticulum; GalNAc, N-acetylgalactosamine; GlcNAc, N-acetylglucosamine; SA, sialic acid; Con A, concanavalin A; AGP, [[alpha].sub.1], acid glycoprotein; CDG, congenital disorders of glycosylation; TRF, transferrin; LAD, leukocyte adhesion deficiency; HEMPAS, hereditary erythroblastic multinuclearity with a positive acidified serum test; WAS, Wiskott-Aldrich syndrome; ALP, alkaline phosphatase; AFP, [alpha]-fetoprotein; and LCA, Lens culinaris agglutinin.
Defect in glycosylation of erythrocyte membrane proteins in congenital dyserythropoietic anaemia type II (HEMPAS).
Congenital dyserythropoietic anaemia type II (HEMPAS) and its molecular basis.