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Year | Number of Results |
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2008 | 1 |
2020 | 1 |
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2024 | 1 |
PubMed (cited) for id: 616023
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SCAF4 variants associated with focal epilepsy accompanied by multisystem disorders.
Seizure. 2024 Mar;116:65-73. doi: 10.1016/j.seizure.2023.06.018. Epub 2023 Jun 22.
Seizure. 2024.
PMID: 37394306
SCAF4-related syndromic intellectual disability.
Carvalho LML, Pinto CF, de Oliveira Scliar M, Otto PA, Krepischi ACV, Rosenberg C.
Carvalho LML, et al.
Am J Med Genet A. 2023 Feb;191(2):570-574. doi: 10.1002/ajmg.a.63032. Epub 2022 Nov 5.
Am J Med Genet A. 2023.
PMID: 36333968
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Variants in SCAF4 Cause a Neurodevelopmental Disorder and Are Associated with Impaired mRNA Processing.
Fliedner A, Kirchner P, Wiesener A, van de Beek I, Waisfisz Q, van Haelst M, Scott DA, Lalani SR, Rosenfeld JA, Azamian MS, Xia F, Dutra-Clarke M, Martinez-Agosto JA, Lee H; UCLA Clinical Genomics Center; Noh GJ, Lippa N, Alkelai A, Aggarwal V, Agre KE, Gavrilova R, Mirzaa GM, Straussberg R, Cohen R, Horist B, Krishnamurthy V, McWalter K, Juusola J, Davis-Keppen L, Ohden L, van Slegtenhorst M, de Man SA, Ekici AB, Gregor A, van de Laar I, Zweier C.
Fliedner A, et al.
Am J Hum Genet. 2020 Sep 3;107(3):544-554. doi: 10.1016/j.ajhg.2020.06.019. Epub 2020 Jul 29.
Am J Hum Genet. 2020.
PMID: 32730804
Free PMC article.
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Snapshots of the RNA processing factor SCAF8 bound to different phosphorylated forms of the carboxyl-terminal domain of RNA polymerase II.
Becker R, Loll B, Meinhart A.
Becker R, et al.
J Biol Chem. 2008 Aug 15;283(33):22659-69. doi: 10.1074/jbc.M803540200. Epub 2008 Jun 11.
J Biol Chem. 2008.
PMID: 18550522
Free article.
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Characterization of cDNA clones selected by the GeneMark analysis from size-fractionated cDNA libraries from human brain.
Hirosawa M, Nagase T, Ishikawa K, Kikuno R, Nomura N, Ohara O.
Hirosawa M, et al.
DNA Res. 1999 Oct 29;6(5):329-36. doi: 10.1093/dnares/6.5.329.
DNA Res. 1999.
PMID: 10574461
Free article.
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