Human Genome Epidemiology Literature Finder
Records 1 - 3 (of 3 Records) |
Query Trace: Syndrome and CLEC16A[original query] |
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Association of the C-type lectin-like domain family-16A (CLEC16A) gene polymorphisms with acute coronary syndrome in Mexican patients. Immunology letters 2014 Dec 162 (2 Pt B): 247-51. Vargas-Alarcon Gilberto, Ramirez-Bello Julian, Angeles-Martinez Javier, Rodriguez-Perez Jose Manuel, Perez-Hernandez Nonanzit, Posadas-Romero Carlos, Jorge-Galarza Esteban, Ocampo-Arcos Wendy Angelica, Obil-Chavarria Claudia, Fragoso Jose Manu |
A variant of CLEC16A gene confers protection for Vogt-Koyanagi-Harada syndrome but not for Behcet's disease in a Chinese Han population. Experimental eye research 2015 Mar 132 225-30. Li Ke, Hou Shengping, Qi Jian, Kijlstra Aize, Yang Peize |
Trio-based exome sequencing and high-resolution HLA typing in families of patients with autoimmune adrenal insufficiency and autoimmune polyglandular syndrome. PloS one 2024 10 19 (10): e0312335. Anastasiia Buianova, Marina Yukina, Valery Cheranev, Oleg Suchalko, Anna Shmitko, Alina Samitova, Nurana Nuralieva, Elena Kulagina, Elena Savvateeva, Ekaterina Troshina, Denis Rebrikov, Dmitry Gryadunov, Dmitriy Korost |
- Page last reviewed:Feb 1, 2024
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