TRAF3 and NBR1 both influence the effect of the disease‐causing CYLD(Arg936X) mutation on NF‐κB activity
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DOI: 10.1111/exd.14365
Abstract: Recently described Hungarian and Anglo‐Saxon pedigrees that are affected by CYLD cutaneous syndrome (syn: Brooke‐Spiegler syndrome (BSS)) carry the same disease‐causing mutation (c.2806C>T, p.Arg936X) of the cylindromatosis (CYLD) gene but exhibit striking phenotypic differences. Using… read more here.
Keywords: traf3 nbr1; cyld arg936x; cyld; effect ... See more keywords