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3. Sheyanth, Inger Norlyk, Højland, Allan Thomas, Okkels, Henrik, Thorup, Christian, Petersen, Michael Bjørn. 2021. First reported CABP2-related non-syndromic hearing loss in Northern Europe. In Molecular genetics & genomic medicine, 9, e1639. doi:10.1002/mgg3.1639. https://pubmed.ncbi.nlm.nih.gov/33666369/
4. Schrauwen, Isabelle, Helfmann, Sarah, Inagaki, Akira, Moser, Tobias, Van Camp, Guy. 2012. A mutation in CABP2, expressed in cochlear hair cells, causes autosomal-recessive hearing impairment. In American journal of human genetics, 91, 636-45. doi:10.1016/j.ajhg.2012.08.018. https://pubmed.ncbi.nlm.nih.gov/22981119/
5. Bharadwaj, Thashi, Schrauwen, Isabelle, Acharya, Anushree, Kotimäki, Jouko, Leal, Suzanne M. 2022. Autosomal recessive nonsyndromic hearing impairment in two Finnish families due to the population enriched CABP2 c.637+1G>T variant. In Molecular genetics & genomic medicine, 10, e1866. doi:10.1002/mgg3.1866. https://pubmed.ncbi.nlm.nih.gov/35150090/
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