A purely quantitative form of partial recessive IFN-γR2 deficiency caused by mutations of the initiation or second codon.
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J. Casanova | C. Deswarte | L. Abel | R. Pérez de Diego | J. Bustamante | S. Boisson-Dupuis | A. Nieto-Patlán | A. Metin | X. Kong | B. Gülhan | R. Martinez-Barricarte | Carmen Oleaga-Quintas | S. Kanık-Yüksek | A. Guérin | M. Moncada-Vélez | Aslınur Özkaya-Parlakay | Indumathi Krishna Rao | S. Murthy