Hyper-IgE Syndrome due to an Elusive Novel Intronic Homozygous Variant in DOCK8
Hyper-IgE Syndrome due to an Elusive Novel Intronic Homozygous Variant in DOCK8
About this item
Full title
Hyper-IgE Syndrome due to an Elusive Novel Intronic Homozygous Variant in DOCK8
Author / Creator
Journal title
Journal of clinical immunology, 2022-01, Vol.42 (1), p.119-129
Language
English
Formats
More information
Alternative Titles
Full title
Hyper-IgE Syndrome due to an Elusive Novel Intronic Homozygous Variant in DOCK8
Authors, Artists and Contributors
Identifiers
Primary Identifiers
Record Identifier
TN_cdi_proquest_miscellaneous_2583317460
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_2583317460
Other Identifiers
ISSN
0271-9142
E-ISSN
1573-2592
DOI
10.1007/s10875-021-01152-x
How to access this item
Log in as a Library member