In silico analysis of all point mutations on the 2B domain of K5/K14 causing epidermolysis bullosa simplex: a genotype–phenotype correlation
Author:
Publisher
Royal Society of Chemistry (RSC)
Subject
Molecular Biology,Biotechnology
Link
http://pubs.rsc.org/en/content/articlepdf/2014/MB/C4MB00138A
Reference19 articles.
1. Elucidating the early stages of keratin filament assembly.
2. Keratin mutations in patients with epidermolysis bullosa simplex: correlations between phenotype severity and disturbance of intermediate filament molecular structure
3. Structural basis for heteromeric assembly and perinuclear organization of keratin filaments
4. The classification of inherited epidermolysis bullosa (EB): Report of the Third International Consensus Meeting on Diagnosis and Classification of EB
5. LIGPLOT: a program to generate schematic diagrams of protein-ligand interactions
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