HuGE Literature Finder
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MRPS18CP2 alleles and DEFA3 absence as putative chromosome 8p23.1 modifiers of hearing loss due to mtDNA mutation A1555G in the 12S rRNA gene. BMC medical genetics 2007 8 (1): 81. Ballana Ester, Mercader Josep Maria, Fischel-Ghodsian Nathan, Estivill Xavi |
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- Page last updated:Aug 16, 2022
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