Researchers discover genetic cause of hearing loss and identify possible treatments
Researchers have understood for decades that some forms of deafness are inherited, yet until now, few of those…
Clinical features and genetic analysis of A20 haploinsufficiency | Orphanet Journal of Rare Diseases
The A20 acts as a critical negative regulator of the NF-κB signaling pathway by suppressing inflammatory cascades through…
A New Cat Color Is Defying Genetic Expectations
“Hearst Magazines and Yahoo may earn commission or revenue on some items through these links.” A new type…