1. van der Velden, J J A J, Jonkman, M F, McLean, W H I, van Steensel, M A M, van Geel, M. 2011. A recurrent mutation in the TGM5 gene in European patients with acral peeling skin syndrome. In Journal of dermatological science, 65, 74-6. doi:10.1016/j.jdermsci.2011.10.002. https://pubmed.ncbi.nlm.nih.gov/22036214/
2. Kiritsi, Dimitra, Cosgarea, Ioana, Franzke, Claus-Werner, Bruckner-Tuderman, Leena, Has, Cristina. 2010. Acral peeling skin syndrome with TGM5 gene mutations may resemble epidermolysis bullosa simplex in young individuals. In The Journal of investigative dermatology, 130, 1741-6. doi:10.1038/jid.2010.23. https://pubmed.ncbi.nlm.nih.gov/20164844/
3. van der Velden, Jaap J A J, van Geel, Michel, Nellen, Ruud G L, McLean, W H Irwin, Cassidy, Andrew J. . Novel TGM5 mutations in acral peeling skin syndrome. In Experimental dermatology, 24, 285-9. doi:10.1111/exd.12650. https://pubmed.ncbi.nlm.nih.gov/25644735/
4. Pigors, Manuela, Kiritsi, Dimitra, Cobzaru, Cristina, Bruckner-Tuderman, Leena, Has, Cristina. 2012. TGM5 mutations impact epidermal differentiation in acral peeling skin syndrome. In The Journal of investigative dermatology, 132, 2422-2429. doi:10.1038/jid.2012.166. https://pubmed.ncbi.nlm.nih.gov/22622422/
5. Grenard, P, Bates, M K, Aeschlimann, D. 2001. Evolution of transglutaminase genes: identification of a transglutaminase gene cluster on human chromosome 15q15. Structure of the gene encoding transglutaminase X and a novel gene family member, transglutaminase Z. In The Journal of biological chemistry, 276, 33066-78. doi:. https://pubmed.ncbi.nlm.nih.gov/11390390/
6. Cangkrama, Michael, Darido, Charbel, Georgy, Smitha R, Wilanowski, Tomasz, Jane, Stephen M. 2016. Two Ancient Gene Families Are Critical for Maintenance of the Mammalian Skin Barrier in Postnatal Life. In The Journal of investigative dermatology, 136, 1438-1448. doi:10.1016/j.jid.2016.02.806. https://pubmed.ncbi.nlm.nih.gov/26975724/
7. Mohamad, Janan, Nanda, Arti, Pavlovsky, Mor, Sprecher, Eli, Sarig, Ofer. 2020. Phenotypic suppression of acral peeling skin syndrome in a patient with autosomal recessive congenital ichthyosis. In Experimental dermatology, 29, 742-748. doi:10.1111/exd.14140. https://pubmed.ncbi.nlm.nih.gov/32618001/