Novel biallelic TRNT1 mutations resulting in sideroblastic anemia, combined B and T cell defects, hypogammaglobulinemia, recurrent infections, hypertrophic cardiomyopathy and developmental delay

Novel biallelic TRNT1 mutations resulting in sideroblastic anemia, combined B and T cell defects, hypogammaglobulinemia, recurrent infections, hypertrophic cardiomyopathy and developmental delay

Détails bibliographiques
Publié dans:Clinical immunology (Orlando, Fla.). - 1999. - 188(2018) vom: 01. März, Seite 20-22
Auteur principal: Lougaris, Vassilios (Auteur)
Autres auteurs: Chou, Janet, Baronio, Manuela, Gazzurelli, Luisa, Lorenzini, Tiziana, Soresina, Annarosa, Moratto, Daniele, Badolato, Raffaele, Seleman, Michael, Bellettato, Massimo, Geha, Raif S, Plebani, Alessandro
Format: Article en ligne
Langue:English
Publié: 2018
Accès à la collection:Clinical immunology (Orlando, Fla.)
Sujets:Case Reports Letter Research Support, Non-U.S. Gov't B cells Hypogammaglobulinemia T cells TRNT1 Nucleotidyltransferases EC 2.7.7.- TRNT1 protein, human EC 2.7.7.72
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