Human Genome Epidemiology Literature Finder
Records 1 - 3 (of 3 Records) |
Query Trace: Abnormalities and PTPN22[original query] |
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Lack of association between the protein tyrosine phosphatase non-receptor 22 (PTPN22)*620W allele and systemic sclerosis in the French Caucasian population. Annals of the rheumatic diseases 2006 Sep 65 (9): 1230-2. Wipff J, Allanore Y, Kahan A, Meyer O, Mouthon L, Guillevin L, Pierlot C, Glikmans E, Bardin T, Boileau C, Cornélis F, Dieudé |
Analysis of PTPN22, ZFAT and MYO9B polymorphisms in Turner Syndrome and risk of autoimmune disease. International journal of immunogenetics 2017 Jun . Villanueva-Ortega E, Ahedo B, Fonseca-Sánchez M A, Pérez-Durán J, Garibay-Nieto N, Macías-Galavíz M T, Trujillo-Cabrera Y, García-Latorre E, Queipo |
Moderating Role of TSHR and PTPN22 Gene Polymorphisms in Effects of Excessive Fluoride on Thyroid: a School-Based Cross-Sectional Study. Biological trace element research 2021 May . Wang Yang, Cui Yushan, Zhang Dandan, Chen Chen, Hou Changchun, Cao Lich |
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