1. Yang, Yuwei, Cao, Yan, Han, Xiaobo, Xiao, Li, Xie, Lixin. 2023. Revealing EXPH5 as a potential diagnostic gene biomarker of the late stage of COPD based on machine learning analysis. In Computers in biology and medicine, 154, 106621. doi:10.1016/j.compbiomed.2023.106621. https://pubmed.ncbi.nlm.nih.gov/36746116/
2. Ostrowski, Matias, Carmo, Nuno B, Krumeich, Sophie, Moita, Luis F, Thery, Clotilde. 2009. Rab27a and Rab27b control different steps of the exosome secretion pathway. In Nature cell biology, 12, 19-30; sup pp 1-13. doi:10.1038/ncb2000. https://pubmed.ncbi.nlm.nih.gov/19966785/
3. Liu, L, Mellerio, J E, Martinez, A E, Parsons, M, McGrath, J A. . Mutations in EXPH5 result in autosomal recessive inherited skin fragility. In The British journal of dermatology, 170, 196-9. doi:10.1111/bjd.12723. https://pubmed.ncbi.nlm.nih.gov/24443915/
4. Bare, Yonis, Chan, Grace K, Hayday, Thomas, McGrath, John A, Parsons, Maddy. 2020. Slac2-b Coordinates Extracellular Vesicle Secretion to Regulate Keratinocyte Adhesion and Migration. In The Journal of investigative dermatology, 141, 523-532.e2. doi:10.1016/j.jid.2020.08.011. https://pubmed.ncbi.nlm.nih.gov/32890627/
5. Malchin, N, Sarig, O, Grafi-Cohen, M, Sprecher, E, Mashiah, J. 2016. A novel homozygous deletion in EXPH5 causes a skin fragility phenotype. In Clinical and experimental dermatology, 41, 915-918. doi:10.1111/ced.12908. https://pubmed.ncbi.nlm.nih.gov/27730671/