A groundbreaking study reveals a genetic mutation that allows some individuals to function optimally on just four hours of sleep. Researchers identified SIK3-N783Y in super sleepers and tested its effects in mice, uncovering potential advancements in sleep disorder treatments.
A groundbreaking study reveals a rare mutation in the SIK3 gene that allows some individuals to thrive on less sleep. Discover how genetics influences our sleep needs and what it could mean for treating sleep disorders.
Emily Kramer-Golinkoff, a cystic fibrosis patient with a rare mutation, highlights the struggles of those left behind as gene therapies show promise for others. Her journey underscores the need for equitable treatments in rare genetic conditions.
A groundbreaking study reveals that a biologic drug may delay Alzheimer's symptoms in individuals with genetic predispositions. With promising results, researchers emphasize the importance of continued funding for further investigation.
New research reveals a single genetic mutation in the NOVA1 gene may explain why humans developed complex speech while Neanderthals could not. This tiny change in a brain protein has vast implications for understanding human communication.
