Autosomal recessive complete STAT1 deficiency caused by compound heterozygous intronic mutations

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Title ( eng )	Autosomal recessive complete STAT1 deficiency caused by compound heterozygous intronic mutations
Title ( jpn )	イントロン領域の複合ヘテロ接合性変異による常染色体劣性STAT1完全欠損症
Creator	Sakata Sonoko
Language	eng
Resource Type	doctoral thesis
Rights	This is a pre-copyedited, author-produced version of an article accepted for publication in International Immunology following peer review. The version of record International Immunology, Volume 32, Issue 10, October 2020, Pages 663-671 is available online at: https://doi.org/10.1093/intimm/dxaa043; https://academic.oup.com/intimm/article/32/10/663/5865324. This is not the published version. Please cite only the published version. この論文は出版社版ではありません。引用の際には出版社版をご確認、ご利用ください。
Publish Type	Not Applicable (or Unknown)
Access Rights	open access
Source Identifier	International Immunology, Volume 32, Issue 10, October 2020, Pages 663-671 [DOI] https://doi.org/10.1093/intimm/dxaa043
Dissertation Number	甲第8279号
Degree Name	Doctor of Philosophy in Medical Science
Date of Granted	2020-08-27
Degree Grantors	広島大学
Remark	Post-print version/PDF may be used in an institutional repository after an embargo period of 12 months.