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. 2018 Oct 17;28(3):524. doi: 10.1093/hmg/ddy357

A purely quantitative form of partial recessive IFN-γR2 deficiency caused by mutations of the initiation or second codon

Carmen Oleaga-Quintas 1,2,3, Caroline Deswarte 1,2, Marcela Moncada-Vélez 4,#, Ayse Metin 5,#, Indumathi Krishna Rao 6,#, Saliha Kanık-Yüksek 5,#, Alejandro Nieto-Patlán 1,2,#, Antoine Guérin 1,2,#, Belgin Gülhan 5,#, Savita Murthy 6,#, Aslınur Özkaya-Parlakay 5,#, Laurent Abel 1,2,7, Rubén Martínez-Barricarte 7, Rebeca Pérez de Diego 8, Stéphanie Boisson-Dupuis 1,2,7,#, Xiao-Fei Kong 7,#, Jean-Laurent Casanova 1,2,7,9,10, Jacinta Bustamante 1,2,7,11,✉
PMCID: PMC6337693  PMID: 30329057

Human Molecular Genetics, 2018, 00(00), xxxx–xxxx.

doi: 10.1093/hmg/ddy275.

In the Abstract, the Greek letter (γ) needs to be added to the term ``IFN-gam,'' they would like to change ``whereas'' to ``and,'' Greek letter (γ) needs to be added to the term ``IFN-gR,'' and the phrase ``with of partial recessive'' should be revised to read ``with of partial recessive.''

The phrase ``...as only one of 18 heterozygous...'' has been changed to ``...as only one of the 18 heterozygous...'' on page 2.

The phrase ``Human Leukocyte Antigen-antigen D Related'' has been revised to ``(HLA-DR)'' on page 5.

The word ``form'' has been changed to ``forms'' on page 11.

The term ``Mycrobacterium chelonei'' is now italicized and changed to read ``Mycobacterium chelonei'' on page 11.

Articles from Human Molecular Genetics are provided here courtesy of Oxford University Press

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