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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1982 1
1987 1
1993 3
1994 2
1996 1
1998 1
1999 1
2001 1
2002 3
2003 5
2004 3
2005 2
2006 1
2007 1
2009 2
2010 3
2011 3
2012 6
2013 5
2015 1
2017 6
2018 1
2019 2
2020 4
2021 6
2023 2
2024 0

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PubMed for id: 1798

55 results

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Page 1
DPAGT1-CDG: Recurrent fetal death.
Tao H, Sun Y, Zhai J, Wu J. Tao H, et al. Birth Defects Res. 2023 Aug 1;115(13):1185-1191. doi: 10.1002/bdr2.2219. Epub 2023 Jul 8. Birth Defects Res. 2023. PMID: 37421173
Clinical features of congenital myasthenic syndrome due to mutations in DPAGT1.
Finlayson S, Palace J, Belaya K, Walls TJ, Norwood F, Burke G, Holton JL, Pascual-Pascual SI, Cossins J, Beeson D. Finlayson S, et al. J Neurol Neurosurg Psychiatry. 2013 Oct;84(10):1119-25. doi: 10.1136/jnnp-2012-304716. Epub 2013 Feb 27. J Neurol Neurosurg Psychiatry. 2013. PMID: 23447650 Free PMC article.
A compound heterozygous mutation in DPAGT1 results in a congenital disorder of glycosylation with a relatively mild phenotype.
Iqbal Z, Shahzad M, Vissers LE, van Scherpenzeel M, Gilissen C, Razzaq A, Zahoor MY, Khan SN, Kleefstra T, Veltman JA, de Brouwer AP, Lefeber DJ, van Bokhoven H, Riazuddin S. Iqbal Z, et al. Eur J Hum Genet. 2013 Aug;21(8):844-9. doi: 10.1038/ejhg.2012.257. Epub 2012 Dec 19. Eur J Hum Genet. 2013. PMID: 23249953 Free PMC article.
55 results