Loss-of-function FERMT1 mutations in kindler syndrome implicate a role for fermitin family homolog-1 in integrin activation
金德勒综合征中 FERMT1 功能丧失突变表明，fermitin 家族同源物-1 在整合素激活中发挥作用。
期刊:American Journal of Pathology
影响因子:3.6
doi:10.2353/ajpath.2009.081154
Lai-Cheong, Joey E; Parsons, Maddy; Tanaka, Akio; Ussar, Siegfried; South, Andrew P; Gomathy, Sethuraman; Mee, John B; Barbaroux, Jean-Baptiste; Techanukul, Tanasit; Almaani, Noor; Clements, Suzanne E; Hart, Ian R; McGrath, John A
