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The causative variants of amyloidosis in the autism.
Int J Neurosci. 2019 Jan;129(1):10-15. doi: 10.1080/00207454.2018.1503177. Epub 2018 Nov 5.
Int J Neurosci. 2019.
PMID: 30074416
PTEN gene mutations in patients with macrocephaly and classic autism: A systematic review.
Zahedi Abghari F, Moradi Y, Akouchekian M.
Zahedi Abghari F, et al.
Med J Islam Repub Iran. 2019 Feb 25;33:10. doi: 10.34171/mjiri.33.10. eCollection 2019.
Med J Islam Repub Iran. 2019.
PMID: 31086789
Free PMC article.
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Long noncoding RNA HOTAIR polymorphisms and susceptibility to bipolar disorder: a preliminary case-control study.
Sargazi S, Zahedi Abghari A, Mirinejad S, Heidari Nia M, Majidpour M, Danesh H, Saravani R, Sheervalilou R, Shakiba M, Zahedi Abghari F.
Sargazi S, et al. Among authors: zahedi abghari f.
Nucleosides Nucleotides Nucleic Acids. 2022;41(7):684-701. doi: 10.1080/15257770.2022.2065017. Epub 2022 Apr 25.
Nucleosides Nucleotides Nucleic Acids. 2022.
PMID: 35469536
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Characterization of Niemann-Pick diseases genes mutation spectrum in Iran and identification of a novel mutation in SMPD1 gene.
Zahedi Abghari F, Bayat F, Razipour M, Karimipoor M, Taghavi-Basmenj M, Zeinali S, Davoudi-Dehaghani E.
Zahedi Abghari F, et al.
Med J Islam Repub Iran. 2019 Nov 25;33:126. doi: 10.34171/mjiri.33.126. eCollection 2019.
Med J Islam Repub Iran. 2019.
PMID: 32280632
Free PMC article.
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