The “Kelch” Surprise: KLHL24, a New Player in the Pathogenesis of Skin Fragility
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Dermatology,Molecular Biology,Biochemistry
Reference11 articles.
1. Degradation of the intermediate filament family by gigaxonin;Bomont;Methods Enzymol,2016
2. Discovery of keratin function and role in genetic diseases: the year that 1991 was;Coulombe;Mol Biol Cell,2016
3. Update on the Kelch-like (KLHL) gene family;Dhanoa;Hum Genomics,2013
4. The genetics of skin fragility;Has;Annu Rev Genomics Hum Genet,2014
5. Monoallelic mutations in the translation initiation codon of KLHL24 cause skin fragility;He;Am J Hum Genet,2016
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