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4. Extremely low penetrance of deafness associated with the mitochondrial 12S rRNA mutation in 16 Chinese families: implication for early detection and prevention of deafness. Dai P; Liu X; Han D; Qian Y; Huang D; Yuan H; Li W; Yu F; Zhang R; Lin H; He Y; Yu Y; Sun Q; Qin H; Li R; Zhang X; Kang D; Cao J; Young WY; Guan MX Biochem Biophys Res Commun; 2006 Feb; 340(1):194-9. PubMed ID: 16375862 [TBL] [Abstract][Full Text] [Related]
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11. Tracking of the genetic deafness associated to the aging in Brazilian patients. Piatto VB; Pereira MC; da Silva MA; Maniglia JV Neurobiol Aging; 2009 Jul; 30(7):1173-4. PubMed ID: 18031868 [TBL] [Abstract][Full Text] [Related]
12. [Correlation between degree of mitochondrial DNA 1555 mutation and clinical phenotype of nonsyndromic hearing loss]. Cheng ZJ; Zhang R; Yang B; Liu QC; Jiang L; Chen J; Chen Y; Ou QS Zhonghua Yi Xue Za Zhi; 2009 Sep; 89(36):2536-9. PubMed ID: 20137613 [TBL] [Abstract][Full Text] [Related]
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