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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

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_2583317460

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

Journal title

Journal of clinical immunology, 2022-01, Vol.42 (1), p.119-129

Language

English

Formats

More information

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

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