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A novel METTL5 variant disrupting a donor splice site leads to primary microcephaly-related intellectual disability in an Iranian family: clinical features and literature review.
J Genet. 2023;102:45.
J Genet. 2023.
PMID: 37731250
Free article.
Review.
X-linked mental retardation-hypotonic facies syndrome: Exome sequencing identifies novel clinical characteristics associated with c.5182G>C mutation in the ATRX gene.
Shakarami F, Jahani M, Nouri Z, Tabatabaiefar MA.
Shakarami F, et al.
Mol Genet Genomic Med. 2022 Oct;10(10):e2034. doi: 10.1002/mgg3.2034. Epub 2022 Aug 13.
Mol Genet Genomic Med. 2022.
PMID: 35962714
Free PMC article.
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Association of plasminogen activator inhibitor-1 and angiotensin converting enzyme polymorphisms with recurrent pregnancy loss in Iranian women.
Shakarami F, Akbari MT, Zare Karizi S.
Shakarami F, et al.
Iran J Reprod Med. 2015 Oct;13(10):627-32.
Iran J Reprod Med. 2015.
PMID: 26644791
Free PMC article.
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Toxoplasma gondii ROP38 protein: Bioinformatics analysis for vaccine design improvement against toxoplasmosis.
Nosrati MC, Ghasemi E, Shams M, Shamsinia S, Yousefi A, Nourmohammadi H, Javanmardi E, Kordi B, Majidiani H, Ghaffari AD, Shakarami F.
Nosrati MC, et al. Among authors: shakarami f.
Microb Pathog. 2020 Dec;149:104488. doi: 10.1016/j.micpath.2020.104488. Epub 2020 Sep 9.
Microb Pathog. 2020.
PMID: 32916240
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