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

Joey E. Lai-Cheong, Maddy Parsons, Akio Tanaka, Siegfried Ussar, Andrew P. South, Sethuraman Gomathy, John B. Mee, Jean-Baptiste Barbaroux, Tanasit Techanukul, Noor Almaani, Suzanne E. Clements, Ian R. Hart, John A. McGrath

Research output: Contribution to journal › Article › peer-review

40 Citations (Scopus)

Fingerprint

Dive into the research topics of 'Loss-of-Function FERMT1 Mutations in Kindler Syndrome Implicate a Role for Fermitin Family Homolog-1 in Integrin Activation'. Together they form a unique fingerprint.

Biochemistry, Genetics and Molecular Biology