Brain organoids reveal mutation-specific insights for Rett syndrome
Teona Gherasim
Picower Institute at MIT Apr 15 2026 Though many studies approach the developmental disorder Rett syndrome as a single condition arising from general loss of function in the gene MECP2, a new study by neuroscientists in The Picower Institute for Learning and Memory at MIT shows that two different mutations of the gene caused many distinct abnormalities in lab cultures. Moreover, correcting key differences made by each mutation required different treatments. " Individual mutations matter ," said
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