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XB-ANAT-254
Papers associated with oocyte (and tmprss3)
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Novel Mutations in the TMPRSS3 Gene may Contribute to Taiwanese Patients with Nonsyndromic Hearing Loss., Wong SH., Int J Mol Sci. March 30, 2020; 21 (7): |
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A novel TMPRSS3 missense mutation in a DFNB8/10 family prevents proteolytic activation of the protein., Wattenhofer M., Hum Genet. October 1, 2005; 117 (6): 528-35. |
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The transmembrane serine protease (TMPRSS3) mutated in deafness DFNB8/10 activates the epithelial sodium channel (ENaC) in vitro., Guipponi M., Hum Mol Genet. November 1, 2002; 11 (23): 2829-36. |
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