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Genotype-phenotype studies in a large cohort of Armenian patients with familial Mediterranean fever suggest clinical disease with heterozygous MEFV mutations.
Moradian MM, Sarkisian T, Ajrapetyan H, Avanesian N. Moradian MM, et al. J Hum Genet. 2010 Jun;55(6):389-93. doi: 10.1038/jhg.2010.52. Epub 2010 May 20. J Hum Genet. 2010. PMID: 20485448
Comprehensive analysis of mutations in the MEFV gene reveal that the location and not the substitution type determines symptom severity in FMF.
Moradian MM, Babikyan D, Banoian D, Hayrapetyan H, Manvelyan H, Avanesian N, Sarkisian T. Moradian MM, et al. Mol Genet Genomic Med. 2017 Nov;5(6):742-750. doi: 10.1002/mgg3.336. Epub 2017 Oct 9. Mol Genet Genomic Med. 2017. PMID: 29178647 Free PMC article.
Patient management and the association of less common familial Mediterranean fever symptoms with other disorders.
Moradian MM, Sarkisian T, Amaryan G, Hayrapetyan H, Yeghiazaryan A, Davidian N, Avanesian N. Moradian MM, et al. Genet Med. 2014 Mar;16(3):258-63. doi: 10.1038/gim.2013.112. Epub 2013 Aug 1. Genet Med. 2014. PMID: 23907647
Complete mitochondrial genome sequence of three Tetrahymena species reveals mutation hot spots and accelerated nonsynonymous substitutions in Ymf genes.
Moradian MM, Beglaryan D, Skozylas JM, Kerikorian V. Moradian MM, et al. PLoS One. 2007 Jul 25;2(7):e650. doi: 10.1371/journal.pone.0000650. PLoS One. 2007. PMID: 17653277 Free PMC article.
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