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2. Genetic analysis of TMPRSS3 gene in the Korean population with autosomal recessive nonsyndromic hearing loss. Lee J; Baek JI; Choi JY; Kim UK; Lee SH; Lee KY Gene; 2013 Dec; 532(2):276-80. PubMed ID: 23958653 [TBL] [Abstract][Full Text] [Related]
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4. Autosomal recessive postlingual hearing loss (DFNB8): compound heterozygosity for two novel TMPRSS3 mutations in German siblings. Elbracht M; Senderek J; Eggermann T; Thürmer C; Park J; Westhofen M; Zerres K J Med Genet; 2007 Jun; 44(6):e81. PubMed ID: 17551081 [TBL] [Abstract][Full Text] [Related]
5. A novel mutation of TMPRSS3 related to milder auditory phenotype in Korean postlingual deafness: a possible future implication for a personalized auditory rehabilitation. Chung J; Park SM; Chang SO; Chung T; Lee KY; Kim AR; Park JH; Kim V; Park WY; Oh SH; Kim D; Park WJ; Choi BY J Mol Med (Berl); 2014 Jun; 92(6):651-63. PubMed ID: 24526180 [TBL] [Abstract][Full Text] [Related]
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9. Mutations in the TMPRSS3 gene are a rare cause of childhood nonsyndromic deafness in Caucasian patients. Wattenhofer M; Di Iorio MV; Rabionet R; Dougherty L; Pampanos A; Schwede T; Montserrat-Sentis B; Arbones ML; Iliades T; Pasquadibisceglie A; D'Amelio M; Alwan S; Rossier C; Dahl HH; Petersen MB; Estivill X; Gasparini P; Scott HS; Antonarakis SE J Mol Med (Berl); 2002 Feb; 80(2):124-31. PubMed ID: 11907649 [TBL] [Abstract][Full Text] [Related]
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11. The Analysis of A Frequent TMPRSS3 Allele Containing P.V116M and P.V291L in A Cis Configuration among Deaf Koreans. Kim AR; Chung J; Kim NKD; Lee C; Park WY; Oh DY; Choi BY Int J Mol Sci; 2017 Oct; 18(11):. PubMed ID: 29072634 [TBL] [Abstract][Full Text] [Related]
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15. GJB2 mutations in Iranian Azeri population with autosomal recessive nonsyndromic hearing loss (ARNSHL): First report of c.238 C>A mutation in Iran. Abbaspour Rodbaneh E; Panahi M; Rahimi B; Mokabber H; Farajollahi R; Davarnia B J Clin Lab Anal; 2021 Nov; 35(11):e24024. PubMed ID: 34581455 [TBL] [Abstract][Full Text] [Related]
17. 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. PubMed ID: 37777971 [TBL] [Abstract][Full Text] [Related]
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