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The histopathology examination assessed fatty degeneration, and degree of fibrosis

Point mutations and NNK site saturation libraries of PtGSTF8 were constructed by overlap extension PCR as previously reported 49 using primers T7 fw, T7 term and: PtGSTF8 (V12X): V12C13_rv and V12X_fw, PtGSTF8 (C13X): V12C13_rv and C13X_fw, PtGSTF8 (C13S): V12C13_rv and C13S_fw, PtGSTF8 (N108X): N108_rv, N108X_fw, PtGSTF8 (F112X): F112_rv, F112X_fw (Supplementary Table 4) using pANT35 as template

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Nyholt et al., Genetic Basis of Male Pattern Baldness, Journal of Investigative Dermatology, 121 (2016), pp.1561-1564

Polycystic ovary syndrome and mental disorders: a systematic review and exploratory meta-analysis