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Four novel p.N385K, p.V36A, c.1033-1034insT and c.1417-1418delCT mutations in the sphingomyelin Phosphodiesterase 1 (SMPD1) gene in patients with types A and B Niemann-Pick disease (NPD).
Manshadi MD, Kamalidehghan B, Keshavarzi F, Aryani O, Dadgar S, Arastehkani A, Tondar M, Ahmadipour F, Meng GY, Houshmand M. Manshadi MD, et al. Among authors: keshavarzi f. Int J Mol Sci. 2015 Mar 24;16(4):6668-76. doi: 10.3390/ijms16046668. Int J Mol Sci. 2015. PMID: 25811928 Free PMC article.
Exome sequencing utility in defining the genetic landscape of hearing loss and novel-gene discovery in Iran.
Mohseni M, Babanejad M, Booth KT, Jamali P, Jalalvand K, Davarnia B, Ardalani F, Khoshaeen A, Arzhangi S, Ghodratpour F, Beheshtian M, Jahanshad F, Otukesh H, Bahrami F, Seifati SM, Bazazzadegan N, Habibi F, Behravan H, Mirzaei S, Keshavarzi F, Nikzat N, Mehrjoo Z, Thiele H, Nothnagel M, Azaiez H, Smith RJ, Kahrizi K, Najmabadi H. Mohseni M, et al. Among authors: keshavarzi f. Clin Genet. 2021 Jul;100(1):59-78. doi: 10.1111/cge.13956. Epub 2021 Mar 24. Clin Genet. 2021. PMID: 33713422 Free PMC article.
Genetic variants linked to T2DM risk in Kurdish populations.
Golsheh S, Keshavarzi F. Golsheh S, et al. Among authors: keshavarzi f. Diabetes Metab Syndr Obes. 2019 Apr 5;12:431-437. doi: 10.2147/DMSO.S189170. eCollection 2019. Diabetes Metab Syndr Obes. 2019. PMID: 31114273 Free PMC article. Retracted.
63 results