博士論文

Autosomal recessive complete STAT1 deficiency caused by compound heterozygous intronic mutations

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Autosomal recessive complete STAT1 deficiency caused by compound heterozygous intronic mutations

Persistent ID (NDL)
info:ndljp/pid/11929832
Material type
博士論文
Author
坂田, 園子
Publisher
-
Publication date
2020-08-27
Material Format
Digital
Capacity, size, etc.
-
Name of awarding university/degree
広島大学,博士(医学),Doctor of Philosophy in Medical Science
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Note (General)：

International Immunology, Volume 32, Issue 10, October 2020, Pages 663-671

Related materials as well as pre- and post-revision versions

International Immunology, Volume 32, Issue 10, October 2020, Pages 663-671

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Digital

Material Type
博士論文
Title
Autosomal recessive complete STAT1 deficiency caused by compound heterozygous intronic mutations
Author/Editor
坂田, 園子
Author Heading
坂田, 園子
Publication Date
2020-08-27
Publication Date (W3CDTF)
2020-08-27
Alternative Title
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
Degree grantor/type
広島大学
Date Granted
2020-08-27
Date Granted (W3CDTF)
2020-08-27