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

Concepedia

Publication | Open Access

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

DOI Full Paper Access

42

Citations

40

References

2009

Year

Joey E. Lai‐Cheong, Maddy Parsons, Akio Tanaka, Siegfried Ussar, Andrew P. South, Gomathy Sethuraman, John Mee, Jean-Baptiste Barbaroux, Tanasit Techanukul, Noor Almaani,

American Journal Of Pathology

GeneticsPathogenesisFermitin Family Homolog-1Molecular BiologyMolecular GeneticsLoss-of-function Fermt1 MutationsMedicineIntegrin Activation

References

	Year	Citations

Page 1

Page 1