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A purely quantitative form of partial recessive IFN-γR2 deficiency caused by mutations of the initiation or second codon
Carmen Oleaga-Quintas, Caroline Deswarte, Marcela Moncada-Vélez, Ayse Metin, Indumathi Krishna Rao, Saliha Kanık-Yüksek, Alejandro Nieto-Patlán, Antoine Guérin, Belgin Gülhan, Savita Murthy, Aslınur Özkaya-Parlakay, Laurent Abel, Rubén Martínez-Barricarte, Rebeca Pérez De Diego, Stéphanie Boisson-Dupuis, Xiao Fei Kong, Jean Laurent Casanova, Jacinta Bustamante
Research output: Contribution to journal › Article › peer-review
16
Scopus
citations