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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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