Etoricoxib

solute carrier organic anion transporter family member 2A1 ; Homo sapiens







4 Article(s)
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1 33852188 Monoallelic mutations in SLCO2A1 cause autosomal dominant primary hypertrophic osteoarthropathy. 2021 Aug 1
2 26875533 Successful treatment of pachydermoperiostosis with etoricoxib in a patient with a homozygous splice-site mutation in the SLCO2A1 gene. 2019 Mar 1
3 29239930 Primary Hypertrophic Osteoarthropathy With SLCO2A1 Mutation in a Chinese Patient Successfully Treated With Etoricoxib. 2018 Apr 1
4 28425581 Clinical, Biochemical, and Genetic Features of 41 Han Chinese Families With Primary Hypertrophic Osteoarthropathy, and Their Therapeutic Response to Etoricoxib: Results From a Six-Month Prospective Clinical Intervention. 2017 Aug 1