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…
Scientists Create Ultimate Antiviral Using Rare “Superpower” Genetic Mutation
A rare genetic mutation that causes a deficiency in an immune regulator called ISG15 is known to make…
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…