Comparative single-cell analysis of biopsies clarifies pathogenic mechanisms in Klinefelter syndrome

Eisa’s paper is now available online in American Journal of Human Genetics. Congratulations! Abstract Klinefelter syndrome (KS), also known as 47, XXY, is characterized by a distinct set of physiological abnormalities, commonly including infertility. The molecular basis for Klinefelter-related infertility is still unclear, largely because of the cellular complexity of the testis and the intricate […]