Unraveling MECP2 structural variants in previously elusive Rett syndrome cases through IGV interpretation
Rett syndrome (RTT) is a severe neurodevelopmental disorder, with MECP2 mutations accounting for 90–95% of classic and 50–70% of atypica…
Rett syndrome (RTT) is a severe neurodevelopmental disorder, with MECP2 mutations accounting for 90–95% of classic and 50–70% of atypica…