1. Rastad, Hadith, Samimisedeh, Parham, Savad, Shahram, Seifi Alan, Mahnaz. 2023. A Novel Exon 2 Deletion Mutation in the GRXCR1 Gene Associated With Non-Syndromic Hearing Loss: A Case Report and Review of Literatures. In The Annals of otology, rhinology, and laryngology, 132, 1493-1495. doi:10.1177/00034894231161866. https://pubmed.ncbi.nlm.nih.gov/37009772/
2. Lorente-Cánovas, Beatriz, Eckrich, Stephanie, Lewis, Morag A, Marcotti, Walter, Steel, Karen P. 2022. Grxcr1 regulates hair bundle morphogenesis and is required for normal mechanoelectrical transduction in mouse cochlear hair cells. In PloS one, 17, e0261530. doi:10.1371/journal.pone.0261530. https://pubmed.ncbi.nlm.nih.gov/35235570/
3. Odeh, Hana, Hunker, Kristina L, Belyantseva, Inna A, Smith, Richard J H, Kohrman, David C. 2010. Mutations in Grxcr1 are the basis for inner ear dysfunction in the pirouette mouse. In American journal of human genetics, 86, 148-60. doi:10.1016/j.ajhg.2010.01.016. https://pubmed.ncbi.nlm.nih.gov/20137774/
4. Schraders, Margit, Lee, Kwanghyuk, Oostrik, Jaap, Leal, Suzanne M, Kremer, Hannie. 2010. Homozygosity mapping reveals mutations of GRXCR1 as a cause of autosomal-recessive nonsyndromic hearing impairment. In American journal of human genetics, 86, 138-47. doi:10.1016/j.ajhg.2009.12.017. https://pubmed.ncbi.nlm.nih.gov/20137778/
5. Mori, Kentaro, Miyanohara, Ikuyo, Moteki, Hideaki, Kurono, Yuichi, Usami, Shin-Ichi. 2015. Novel mutation in GRXCR1 at DFNB25 lead to progressive hearing loss and dizziness. In The Annals of otology, rhinology, and laryngology, 124 Suppl 1, 129S-34S. doi:10.1177/0003489415575061. https://pubmed.ncbi.nlm.nih.gov/25802247/
6. Avenarius, Matthew R, Jung, Jae-Yun, Askew, Charles, Raphael, Yehoash, Kohrman, David C. 2018. Grxcr2 is required for stereocilia morphogenesis in the cochlea. In PloS one, 13, e0201713. doi:10.1371/journal.pone.0201713. https://pubmed.ncbi.nlm.nih.gov/30157177/
7. Šafka Brožková, Dana, Laštůvková, Jana, Machalová, Eliška, Trková, Marie, Seeman, Pavel. 2012. DFNB35 due to a novel mutation in the ESRRB gene in a Czech consanguineous family. In International journal of pediatric otorhinolaryngology, 76, 1681-4. doi:10.1016/j.ijporl.2012.08.006. https://pubmed.ncbi.nlm.nih.gov/22951369/
8. Khan, Amjad, Han, Shirui, Wang, Rongrong, Ahmad, Wasim, Zhang, Xue. 2019. Sequence variants in genes causing nonsyndromic hearing loss in a Pakistani cohort. In Molecular genetics & genomic medicine, 7, e917. doi:10.1002/mgg3.917. https://pubmed.ncbi.nlm.nih.gov/31389194/