1. Xu, Liangpu, Wang, Xinrui, Li, Jia, Huang, Hailong, Cao, Hua. 2023. A novel PLS1 c.981+1G>A variant causes autosomal-dominant hereditary hearing loss in a family. In Clinical genetics, 103, 413-423. doi:10.1111/cge.14283. https://pubmed.ncbi.nlm.nih.gov/36537221/
2. Clergeot, P H, Gourgues, M, Cots, J, Notteghem, J L, Lebrun, M H. . PLS1, a gene encoding a tetraspanin-like protein, is required for penetration of rice leaf by the fungal pathogen Magnaporthe grisea. In Proceedings of the National Academy of Sciences of the United States of America, 98, 6963-8. doi:. https://pubmed.ncbi.nlm.nih.gov/11391010/
3. Schrauwen, Isabelle, Melegh, Béla I, Chakchouk, Imen, Melegh, Béla, Leal, Suzanne M. 2019. Hearing impairment locus heterogeneity and identification of PLS1 as a new autosomal dominant gene in Hungarian Roma. In European journal of human genetics : EJHG, 27, 869-878. doi:10.1038/s41431-019-0372-y. https://pubmed.ncbi.nlm.nih.gov/30872814/
4. Veneault-Fourrey, Claire, Lambou, Karine, Lebrun, Marc-Henri. . Fungal Pls1 tetraspanins as key factors of penetration into host plants: a role in re-establishing polarized growth in the appressorium? In FEMS microbiology letters, 256, 179-84. doi:. https://pubmed.ncbi.nlm.nih.gov/16499604/
5. Morgan, Anna, Koboldt, Daniel C, Barrie, Elizabeth S, Dell'Orco, Daniele, Girotto, Giorgia. 2019. Mutations in PLS1, encoding fimbrin, cause autosomal dominant nonsyndromic hearing loss. In Human mutation, 40, 2286-2295. doi:10.1002/humu.23891. https://pubmed.ncbi.nlm.nih.gov/31397523/
6. Diaz-Horta, Oscar, Bademci, Guney, Tokgoz-Yilmaz, Suna, Farooq, Amjad, Tekin, Mustafa. 2019. Novel variant p.E269K confirms causative role of PLS1 mutations in autosomal dominant hearing loss. In Clinical genetics, 96, 575-578. doi:10.1111/cge.13626. https://pubmed.ncbi.nlm.nih.gov/31432506/
7. Yao, Guanqun, Zou, Ting, Luo, Jing, Xu, Yong, Liu, Pozi. 2023. Cortical structural changes of morphometric similarity network in early-onset schizophrenia correlate with specific transcriptional expression patterns. In BMC medicine, 21, 479. doi:10.1186/s12916-023-03201-1. https://pubmed.ncbi.nlm.nih.gov/38049797/
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