Homo sapiens clone c.218G>A transmembrane protease serine 3 (TMPRSS3) - Nucleotide

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[Late-onset hereditary hearing loss caused by TMPRSS3 compound heterozygous mutations]. [Lin Chuang Er Bi Yan Hou Tou J...]
[Late-onset hereditary hearing loss caused by TMPRSS3 compound heterozygous mutations].
Wang Y, Liang Y, Huang B, Cen X, Huang L, Chen K. Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2024 Aug; 38(8):679-686.
Homozygous Missense Variants in FOXI1 and TMPRSS3 Genes Associated with Non-syndromic Deafness in Moroccan Families. [Biochem Genet. 2024]
Homozygous Missense Variants in FOXI1 and TMPRSS3 Genes Associated with Non-syndromic Deafness in Moroccan Families.
AitRaise I, Amalou G, Bakhchane A, Bousfiha A, Abdelghaffar H, Majida C, Bonnet C, Petit C, Barakat A. Biochem Genet. 2024 Jun; 62(3):1914-1924. Epub 2023 Oct 1.
Genotype-Phenotype Correlations in TMPRSS3 (DFNB10/DFNB8) with Emphasis on Natural History. [Audiol Neurootol. 2023]
Genotype-Phenotype Correlations in TMPRSS3 (DFNB10/DFNB8) with Emphasis on Natural History.
Nisenbaum E, Yan D, Shearer AE, de Joya E, Thielhelm T, Russell N, Staecker H, Chen Z, Holt JR, Liu X. Audiol Neurootol. 2023; 28(6):407-419. Epub 2023 Jun 16.