Human Genome Epidemiology Literature Finder
Records 1 - 2 (of 2 Records) |
Query Trace: CLDN23[original query] |
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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 |
Multiple signals at the extended 8p23 locus are associated with susceptibility to systemic lupus erythematosus. Journal of medical genetics 2017 Mar . Demirci F Yesim, Wang Xingbin, Morris David L, Feingold Eleanor, Bernatsky Sasha, Pineau Christian, Clarke Ann, Ramsey-Goldman Rosalind, Manzi Susan, Vyse Timothy J, Ilyas Kamboh |
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