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7. Ramzan, Khushnooda, Al-Owain, Mohammed, Allam, Rabab, Taibah, Khalid, Imtiaz, Faiqa. 2013. Homozygosity mapping identifies a novel GIPC3 mutation causing congenital nonsyndromic hearing loss in a Saudi family. In Gene, 521, 195-9. doi:10.1016/j.gene.2013.03.042. https://pubmed.ncbi.nlm.nih.gov/23510777/
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