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Major histocompatibility complex class II expression deficiency caused by a RFXANK founder mutation: a survey of 35 patients.

Authors
Type
Published Article
Journal
Blood
1528-0020
Publisher
American Society of Hematology
Publication Date
Volume
118
Issue
19
Pages
5108–5118
Identifiers
DOI: 10.1182/blood-2011-05-352716
PMID: 21908431
Source
Medline

Abstract

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