Analysis of GABRG2 C588T polymorphism in genetic epilepsy and evaluation of GABRG2 in drug treatment

Abstract Epilepsy is a common disorder with complex inheritance, and its treatment is very unsatisfactory. An association between the GABRG2 C588T polymorphism and genetic generalized epilepsy has been studied by several genetic association studies. However, these results were inconsistent, and the...

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Päätekijät: Shitao Wang (Tekijä), Xianjun Zhang (Tekijä), Liang Zhou (Tekijä), Qian Wu (Tekijä), Yanbing Han (Tekijä)
Aineistotyyppi: Kirja
Julkaistu: Wiley, 2021-09-01T00:00:00Z.
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