Investigation of Transcription Factor and Cytokine Gene Expression Levels in Helper T Cell Subsets A...
Investigation of Transcription Factor and Cytokine Gene Expression Levels in Helper T Cell Subsets Among Turkish Patients Diagnosed with ICF2 (Novel ZBTB24 gene Variant) and ICF3 (CDCA7 Variant) Syndrome
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Publisher
New York: Springer US
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Language
English
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Publisher
New York: Springer US
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Contents
Immunodeficiency, centromeric region instability, facial anomalies syndrome (ICF), is a rare disease with autosomal recessive inheritance. ICF syndrome. It has been reported that ICF syndrome is caused by mutations in the
DNMT3B
(ICF1),
ZBTB24
(ICF2),
CDCA7
(ICF3), and
HELLS
(ICF4) genes. As a result of literature research,...
Alternative Titles
Full title
Investigation of Transcription Factor and Cytokine Gene Expression Levels in Helper T Cell Subsets Among Turkish Patients Diagnosed with ICF2 (Novel ZBTB24 gene Variant) and ICF3 (CDCA7 Variant) Syndrome
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TN_cdi_proquest_miscellaneous_3153810371
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_3153810371
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ISSN
0271-9142,1573-2592
E-ISSN
1573-2592
DOI
10.1007/s10875-024-01807-5
