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P792: CRISPR/CAS9-BASED MODEL OF HETEROZYGOUS CXCR4 WT/R334X MUTATION TO STUDY CELLULAR PHENOTYPES IN WHIM SYNDROME

Detalles Bibliográficos
Autores principales: Zmajkovicova, K., Pawar, S., Maier-Munsa, S., Badarau, A., Taveras, A. G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9429556/
http://dx.doi.org/10.1097/01.HS9.0000846052.61635.87
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author Zmajkovicova, K.
Pawar, S.
Maier-Munsa, S.
Badarau, A.
Taveras, A. G.
author_facet Zmajkovicova, K.
Pawar, S.
Maier-Munsa, S.
Badarau, A.
Taveras, A. G.
author_sort Zmajkovicova, K.
collection PubMed
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spelling pubmed-94295562022-08-31 P792: CRISPR/CAS9-BASED MODEL OF HETEROZYGOUS CXCR4 WT/R334X MUTATION TO STUDY CELLULAR PHENOTYPES IN WHIM SYNDROME Zmajkovicova, K. Pawar, S. Maier-Munsa, S. Badarau, A. Taveras, A. G. Hemasphere Posters Lippincott Williams & Wilkins 2022-06-23 /pmc/articles/PMC9429556/ http://dx.doi.org/10.1097/01.HS9.0000846052.61635.87 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 Posters
Zmajkovicova, K.
Pawar, S.
Maier-Munsa, S.
Badarau, A.
Taveras, A. G.
P792: CRISPR/CAS9-BASED MODEL OF HETEROZYGOUS CXCR4 WT/R334X MUTATION TO STUDY CELLULAR PHENOTYPES IN WHIM SYNDROME
title P792: CRISPR/CAS9-BASED MODEL OF HETEROZYGOUS CXCR4 WT/R334X MUTATION TO STUDY CELLULAR PHENOTYPES IN WHIM SYNDROME
title_full P792: CRISPR/CAS9-BASED MODEL OF HETEROZYGOUS CXCR4 WT/R334X MUTATION TO STUDY CELLULAR PHENOTYPES IN WHIM SYNDROME
title_fullStr P792: CRISPR/CAS9-BASED MODEL OF HETEROZYGOUS CXCR4 WT/R334X MUTATION TO STUDY CELLULAR PHENOTYPES IN WHIM SYNDROME
title_full_unstemmed P792: CRISPR/CAS9-BASED MODEL OF HETEROZYGOUS CXCR4 WT/R334X MUTATION TO STUDY CELLULAR PHENOTYPES IN WHIM SYNDROME
title_short P792: CRISPR/CAS9-BASED MODEL OF HETEROZYGOUS CXCR4 WT/R334X MUTATION TO STUDY CELLULAR PHENOTYPES IN WHIM SYNDROME
title_sort p792: crispr/cas9-based model of heterozygous cxcr4 wt/r334x mutation to study cellular phenotypes in whim syndrome
topic Posters
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9429556/
http://dx.doi.org/10.1097/01.HS9.0000846052.61635.87
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