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Results by year

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

Year Number of Results
1973 1
1991 1
1992 1
1993 1
1994 3
1995 1
1997 1
1998 2
1999 1
2001 3
2002 3
2003 3
2004 7
2005 6
2006 4
2007 4
2008 8
2009 12
2010 17
2011 23
2012 17
2013 22
2014 14
2015 29
2016 15
2017 18
2018 30
2019 34
2020 29
2021 27
2022 48
2023 22
2024 2

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PubMed for id: 498

360 results

Results by year

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Page 1
A recurrent de novo ATP5F1A substitution associated with neonatal complex V deficiency.
Lines MA, Cuillerier A, Chakraborty P, Naas T, Duque Lasio ML, Michaud J, Pileggi C, Harper ME, Burelle Y, Toler TL, Sondheimer N, Crawford HP, Millan F, Geraghty MT. Lines MA, et al. Eur J Hum Genet. 2021 Nov;29(11):1719-1724. doi: 10.1038/s41431-021-00956-0. Epub 2021 Sep 6. Eur J Hum Genet. 2021. PMID: 34483339 Free PMC article.
Targeted exome sequencing of suspected mitochondrial disorders.
Lieber DS, Calvo SE, Shanahan K, Slate NG, Liu S, Hershman SG, Gold NB, Chapman BA, Thorburn DR, Berry GT, Schmahmann JD, Borowsky ML, Mueller DM, Sims KB, Mootha VK. Lieber DS, et al. Neurology. 2013 May 7;80(19):1762-70. doi: 10.1212/WNL.0b013e3182918c40. Epub 2013 Apr 17. Neurology. 2013. PMID: 23596069 Free PMC article.
360 results