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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:	Posters
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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