Author:
Bolling Marieke C.,Jongbloed Jan D.H.,Boven Ludolf G.,Diercks Gilles F.H.,Smith Frances J.D.,Irwin McLean W.H.,Jonkman Marcel F.
Subject
Cell Biology,Dermatology,Molecular Biology,Biochemistry
Reference16 articles.
1. Mutations in KRT5 and KRT14 cause epidermolysis bullosa simplex in 75% of the patients;Bolling;Br J Dermatol,2011
2. Structures of two intermediate filament-binding fragments of desmoplakin reveal a unique repeat motif structure;Choi;Nat Struc Biol,2002
3. Point mutations in human keratin 14 genes of epidermolysis bullosa simplex patients: genetic and functional analyses;Coulombe;Cell,1991
4. Epidermolysis Bullosa: A Clinical, Genetic and Epidemiological Study;Gedde-Dahl,1971
5. Plectin repeats and modules: strategic cysteines and their presumed impact on cytolinker functions;Janda;Bioessays,2001
Cited by
36 articles.
订阅此论文施引文献
订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献