Loss-of-Function FERMT1 Mutations in Kindler Syndrome Implicate a Role for Fermitin Family Homolog-1 in Integrin Activation

par 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.
Publié 2009