. . . . . . . "[The incidence of leptin gene G2548A homozygous mutant AA polymorphism was significantly increased in the OSCC patients (p?=?0.002, odds ratio (OR)?=?2.4, 95 % confidence interval (CI)?=?1.37-4.22) when compared with controls, and leptin receptor A668G homozygous mutant GG polymorphism was significantly high in the OSCC patients as compared to controls (p?=?0.000, OR?=?3.8, 95 % CI?=?1.98-7.62).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en . . . . . "2017-02-19"^^ . . "Gene-disease associations inferred from text-mining the literature."@en . "DisGeNET evidence - LITERATURE"@en . "2017-10-17T13:14:17+02:00"^^ . . . . . . . . . . . "v5.0.0.0" . "v5.0.0" .