Clinical impact of the TPSAB1 genotype in mast cell diseases: A REMA study in a cohort of 959 individuals

Background A close association between hereditary alpha‐tryptasemia (HAT) and mast cell (MC) disorders has been previously reported. However, the relationship between HAT and the diagnostic subtypes and clinical features of MC disorders still remains to be established. Objective To determine the pre...

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Veröffentlicht in:	Allergy (Copenhagen) 2024-03, Vol.79 (3), p.711-723
Hauptverfasser:	González‐de‐Olano, David, Navarro‐Navarro, Paula, Muñoz‐González, Javier I., Sánchez‐Muñoz, Laura, Henriques, Ana, de‐Andrés‐Martín, Ana, Peralta‐Arjonilla, Dolores, Mayado, Andrea, Jara‐Acevedo, María, García‐Montero, Andrés C., Orfao, Alberto, Álvarez‐Twose, Iván
Format:	Artikel
Sprache:	eng
Schlagworte:	Anaphylaxis copy number mutation Disease frequency Genotypes HAT Mastocytosis Tryptase
Online-Zugang:	Volltext
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