A purely quantitative form of partial recessive IFN-γR2 deficiency caused by mutations of the initiation or second codon (vol 27, pg 3919, 2018)

Oleaga-Quintas C., Deswarte C., Moncada-Vélez M., Metin A., Rao I. K., Kanık Yüksek S., ...More

Human Molecular Genetics, vol.27, no.22, pp.3919-3935, 2019 (Peer-Reviewed Journal)

• Publication Type: Article / Article
• Volume: 27 Issue: 22
• Publication Date: 2019
• Doi Number: 10.1093/hmg/ddy357
• Journal Name: Human Molecular Genetics
• Page Numbers: pp.3919-3935
• Open Archive Collection: AVESIS Open Access Collection
• Ankara Yıldırım Beyazıt University Affiliated: Yes