PB2295: EVANS SYNDROME AND PHENOTYPIC HETEROGENEITY OF SASH3 GERMLINE LOSS-OF-FUNCTION MUTATIONS BEYOND X-LINKED IMMUNODEFICIENCY

Detalles Bibliográficos
Autores principales: Berner, J., Novak, W., Jimenez-Heredia, R., Kager, L., Boztug, K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2022
Materias:
Publication Only
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9431601/
http://dx.doi.org/10.1097/01.HS9.0000852008.57011.e7
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author Berner, J.
Novak, W.
Jimenez-Heredia, R.
Kager, L.
Boztug, K.
author_facet Berner, J.
Novak, W.
Jimenez-Heredia, R.
Kager, L.
Boztug, K.
author_sort Berner, J.
collection PubMed
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spelling pubmed-94316012022-08-31 PB2295: EVANS SYNDROME AND PHENOTYPIC HETEROGENEITY OF SASH3 GERMLINE LOSS-OF-FUNCTION MUTATIONS BEYOND X-LINKED IMMUNODEFICIENCY Berner, J. Novak, W. Jimenez-Heredia, R. Kager, L. Boztug, K. Hemasphere Publication Only Lippincott Williams & Wilkins 2022-06-23 /pmc/articles/PMC9431601/ http://dx.doi.org/10.1097/01.HS9.0000852008.57011.e7 Text en Copyright © 2022 The Author(s). Published by Wolters Kluwer Health, Inc. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access Abstract Book distributed under the Attribution-NonCommercial-NoDerivs (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) which allows third parties to download the articles and share them with others as long as they credit the author and the Abstract Book, but they cannot change the content in any way or use them commercially.
spellingShingle Publication Only
Berner, J.
Novak, W.
Jimenez-Heredia, R.
Kager, L.
Boztug, K.
PB2295: EVANS SYNDROME AND PHENOTYPIC HETEROGENEITY OF SASH3 GERMLINE LOSS-OF-FUNCTION MUTATIONS BEYOND X-LINKED IMMUNODEFICIENCY
title PB2295: EVANS SYNDROME AND PHENOTYPIC HETEROGENEITY OF SASH3 GERMLINE LOSS-OF-FUNCTION MUTATIONS BEYOND X-LINKED IMMUNODEFICIENCY
title_full PB2295: EVANS SYNDROME AND PHENOTYPIC HETEROGENEITY OF SASH3 GERMLINE LOSS-OF-FUNCTION MUTATIONS BEYOND X-LINKED IMMUNODEFICIENCY
title_fullStr PB2295: EVANS SYNDROME AND PHENOTYPIC HETEROGENEITY OF SASH3 GERMLINE LOSS-OF-FUNCTION MUTATIONS BEYOND X-LINKED IMMUNODEFICIENCY
title_full_unstemmed PB2295: EVANS SYNDROME AND PHENOTYPIC HETEROGENEITY OF SASH3 GERMLINE LOSS-OF-FUNCTION MUTATIONS BEYOND X-LINKED IMMUNODEFICIENCY
title_short PB2295: EVANS SYNDROME AND PHENOTYPIC HETEROGENEITY OF SASH3 GERMLINE LOSS-OF-FUNCTION MUTATIONS BEYOND X-LINKED IMMUNODEFICIENCY
title_sort pb2295: evans syndrome and phenotypic heterogeneity of sash3 germline loss-of-function mutations beyond x-linked immunodeficiency
topic Publication Only
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9431601/
http://dx.doi.org/10.1097/01.HS9.0000852008.57011.e7
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