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The Non-Synonymous C1858T Substitution in the PTPN22 Gene is Associated with Susceptibility to the Severe Forms of Alopecia Areata

✍ Scribed by E. Helen Kemp; Andrew J.G. McDonagh; David A. Wengraf; Andrew G. Messenger; David J. Gawkrodger; Michael J. Cork; Rachid Tazi-Ahnini


Book ID
116531112
Publisher
Elsevier Science
Year
2006
Tongue
English
Weight
94 KB
Volume
67
Category
Article
ISSN
0198-8859

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## Abstract ## Objective Variants in genes encoding the Fc receptor–like 3 (FcRL‐3) and the class II major histocompatibility complex (MHC) transactivator proteins have been associated with an increased risk of rheumatoid arthritis (RA) in Japanese and Nordic populations, respectively. The aim of