Homo sapiens cDNA FLJ50607 complete cds, highly similar to Pendrin

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Low frequency of SLC26A4 c.919-2A > G variant among patients with nonsyndromic hearing loss in Yunnan of Southwest China. [BMC Med Genomics. 2024]
Low frequency of SLC26A4 c.919-2A > G variant among patients with nonsyndromic hearing loss in Yunnan of Southwest China.
Li YQ, Ma H, Wang QY, Liu DS, Wang W, Li SX, Zuo RX, Shen T, Zhu BS, Sa YL. BMC Med Genomics. 2024 Feb 20; 17(1):55. Epub 2024 Feb 20.
Mutation analysis of GJB2, SLC26A4, GJB3 and mtDNA12SrRNA genes in 251 non-syndromic hearing loss patients in Fujian, China. [Int J Pediatr Otorhinolaryngol...]
Mutation analysis of GJB2, SLC26A4, GJB3 and mtDNA12SrRNA genes in 251 non-syndromic hearing loss patients in Fujian, China.
Xiong Y, Chen M, Wang H, Chen L, Huang H, Xu L. Int J Pediatr Otorhinolaryngol. 2024 Jan; 176:111777. Epub 2023 Nov 21.
Dispersed DNA variants underlie hearing loss in South Florida's minority population. [Hum Genomics. 2023]
Dispersed DNA variants underlie hearing loss in South Florida's minority population.
Peart L, Gonzalez J, Morel Swols D, Duman D, Saridogan T, Ramzan M, Zafeer MF, Liu XZ, Eshraghi AA, Hoffer ME, et al. Hum Genomics. 2023 Nov 24; 17(1):103. Epub 2023 Nov 24.

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Nucleotide