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hKCa3/KCNN3 potassium channel gene: association of longer CAG repeats with schizophrenia in Israeli Ashkenazi Jews, expression in human tissues and localization to chromosome 1q21.
Dror V, Shamir E, Ghanshani S, Kimhi R, Swartz M, Barak Y, Weizman R, Avivi L, Litmanovitch T, Fantino E, Kalman K, Jones EG, Chandy KG, Gargus JJ, Gutman GA, Navon R. Dror V, et al. Among authors: navon r. Mol Psychiatry. 1999 May;4(3):254-60. doi: 10.1038/sj.mp.4000508. Mol Psychiatry. 1999. PMID: 10395215
Estimation of the mutation frequencies in Charcot-Marie-Tooth disease type 1 and hereditary neuropathy with liability to pressure palsies: a European collaborative study.
Nelis E, Van Broeckhoven C, De Jonghe P, Löfgren A, Vandenberghe A, Latour P, Le Guern E, Brice A, Mostacciuolo ML, Schiavon F, Palau F, Bort S, Upadhyaya M, Rocchi M, Archidiacono N, Mandich P, Bellone E, Silander K, Savontaus ML, Navon R, Goldberg-Stern H, Estivill X, Volpini V, Friedl W, Gal A, et al. Nelis E, et al. Among authors: navon r. Eur J Hum Genet. 1996;4(1):25-33. doi: 10.1159/000472166. Eur J Hum Genet. 1996. PMID: 8800924 Free article.
Is the WKL1 gene associated with schizophrenia?
Kaganovich M, Peretz A, Ritsner M, Bening Abu-Shach U, Attali B, Navon R. Kaganovich M, et al. Among authors: navon r. Am J Med Genet B Neuropsychiatr Genet. 2004 Feb 15;125B(1):31-7. doi: 10.1002/ajmg.b.20115. Am J Med Genet B Neuropsychiatr Genet. 2004. PMID: 14755440
Transmission disequilibrium and haplotype analyses of the G72/G30 locus: suggestive linkage to schizophrenia in Palestinian Arabs living in the North of Israel.
Korostishevsky M, Kremer I, Kaganovich M, Cholostoy A, Murad I, Muhaheed M, Bannoura I, Rietschel M, Dobrusin M, Bening-Abu-Shach U, Belmaker RH, Maier W, Ebstein RP, Navon R. Korostishevsky M, et al. Among authors: navon r. Am J Med Genet B Neuropsychiatr Genet. 2006 Jan 5;141B(1):91-5. doi: 10.1002/ajmg.b.30212. Am J Med Genet B Neuropsychiatr Genet. 2006. PMID: 16082701
121 results