Homo sapiens mast cell beta I tryptase mRNA, partial cds, alternativel - Nucleotide

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Clinical impact of the TPSAB1 genotype in mast cell diseases: A REMA study in a cohort of 959 individuals. [Allergy. 2024]
Clinical impact of the TPSAB1 genotype in mast cell diseases: A REMA study in a cohort of 959 individuals.
González-de-Olano D, Navarro-Navarro P, Muñoz-González JI, Sánchez-Muñoz L, Henriques A, de-Andrés-Martín A, Peralta-Arjonilla D, Mayado A, Jara-Acevedo M, García-Montero AC, et al. Allergy. 2024 Mar; 79(3):711-723. Epub 2023 Oct 11.
Hereditary α tryptasemia is a valid genetic biomarker for severe mediator-related symptoms in mastocytosis. [Blood. 2021]
Hereditary α tryptasemia is a valid genetic biomarker for severe mediator-related symptoms in mastocytosis.
Greiner G, Sprinzl B, Górska A, Ratzinger F, Gurbisz M, Witzeneder N, Schmetterer KG, Gisslinger B, Uyanik G, Hadzijusufovic E, et al. Blood. 2021 Jan 14; 137(2):238-247.
Heritable risk for severe anaphylaxis associated with increased α-tryptase-encoding germline copy number at TPSAB1. [J Allergy Clin Immunol. 2021]
Heritable risk for severe anaphylaxis associated with increased α-tryptase-encoding germline copy number at TPSAB1.
Lyons JJ, Chovanec J, O'Connell MP, Liu Y, Šelb J, Zanotti R, Bai Y, Kim J, Le QT, DiMaggio T, et al. J Allergy Clin Immunol. 2021 Feb; 147(2):622-632. Epub 2020 Jul 24.

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Nucleotide