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Monoclonal Gammopathy of Unclear Significance in a Child with Wiskott-Aldrich Syndrome: a Rare Occur...

Monoclonal Gammopathy of Unclear Significance in a Child with Wiskott-Aldrich Syndrome: a Rare Occur...

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_2164101024

Monoclonal Gammopathy of Unclear Significance in a Child with Wiskott-Aldrich Syndrome: a Rare Occurrence

About this item

Full title

Monoclonal Gammopathy of Unclear Significance in a Child with Wiskott-Aldrich Syndrome: a Rare Occurrence

Journal title

Journal of clinical immunology, 2019, Vol.39 (1), p.7-10

Language

English

Formats

More information

Alternative Titles

Full title

Monoclonal Gammopathy of Unclear Significance in a Child with Wiskott-Aldrich Syndrome: a Rare Occurrence

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_proquest_miscellaneous_2164101024

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_2164101024

Other Identifiers

E-ISSN

1573-2592

DOI

10.1007/s10875-018-0585-9

How to access this item