【霸氣阿宏】評論
Meta-analysis of eight genome-wide association studies has identified at least six genomic regions that are statistically associated with endometriosis [52]. In addition, a study that analyzed exome sequencing of non-malignant deep endometriosis lesions reported somatic mutations in 79 percent of lesions and mutations in the known cancer driver genes ARID1A, PIK3CA, KRAS, and PPP2R1A in 26 percent of lesions.