Published in
Oxford University Press, Human Molecular Genetics, 2018
DOI: 10.1093/hmg/ddy275
Oxford University Press (OUP), Human Molecular Genetics, 3(28), p. 524-524, 2018
DOI: 10.1093/hmg/ddy357
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A purely quantitative form of partial recessive IFN-γR2 deficiency caused by mutations of the initiation or second codon
Journal article published in 2018 by
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 
and other authors.
and other authors.
This paper was not found in any repository, but could be made available legally by the author.
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