Human Genome Epidemiology Literature Finder
Records 1 - 2 (of 2 Records) |
Query Trace: CACNG3[original query] |
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Linkage and association analysis of CACNG3 in childhood absence epilepsy. European journal of human genetics : EJHG 2007 Apr 15 (4): 463-72. Everett Kate V, Chioza Barry, Aicardi Jean, Aschauer Harald, Brouwer Oebele, Callenbach Petra, Covanis Athanasios, Dulac Olivier, Eeg-Olofsson Orvar, Feucht Martha, Friis Mogens, Goutieres Françoise, Guerrini Renzo, Heils Armin, Kjeldsen Marianne, Lehesjoki Anna-Elina, Makoff Andrew, Nabbout Rima, Olsson Ingrid, Sander Thomas, Sirén Auli, McKeigue Paul, Robinson Robert, Taske Nichole, Rees Michele, Gardiner Ma |
Dissection of chromosome 16p12 linkage peak suggests a possible role for CACNG3 variants in age-related macular degeneration susceptibility. Investigative ophthalmology & visual science 2011 Mar 52 (3): 1748-54. Spencer Kylee L, Olson Lana M, Schnetz-Boutaud Nathalie, Gallins Paul, Wang Gaofeng, Scott William K, Agarwal Anita, Jakobsdottir Johanna, Conley Yvette, Weeks Daniel E, Gorin Michael B, Pericak-Vance Margaret A, Haines Jonathan |
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