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

Year Number of Results
1988 1
1998 2
2000 1
2001 1
2002 6
2003 1
2004 1
2006 1
2007 2
2008 2
2009 1
2010 4
2011 6
2012 4
2013 4
2014 2
2015 2
2016 6
2017 6
2018 3
2019 9
2020 4
2021 8
2022 7
2023 4
2024 1

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PubMed for id: 400428

77 results

Results by year

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Page 1
BCS1L gene mutation causing GRACILE syndrome: case report.
Kasapkara ÇS, Tümer L, Ezgü FS, Küçükçongar A, Hasanoğlu A. Kasapkara ÇS, et al. Ren Fail. 2014 Jul;36(6):953-4. doi: 10.3109/0886022X.2014.900422. Epub 2014 Mar 24. Ren Fail. 2014. PMID: 24655110
Alternative oxidase-mediated respiration prevents lethal mitochondrial cardiomyopathy.
Rajendran J, Purhonen J, Tegelberg S, Smolander OP, Mörgelin M, Rozman J, Gailus-Durner V, Fuchs H, Hrabe de Angelis M, Auvinen P, Mervaala E, Jacobs HT, Szibor M, Fellman V, Kallijärvi J. Rajendran J, et al. EMBO Mol Med. 2019 Jan;11(1):e9456. doi: 10.15252/emmm.201809456. EMBO Mol Med. 2019. PMID: 30530468 Free PMC article.
Respiratory chain complex III deficiency due to mutated BCS1L: a novel phenotype with encephalomyopathy, partially phenocopied in a Bcs1l mutant mouse model.
Tegelberg S, Tomašić N, Kallijärvi J, Purhonen J, Elmér E, Lindberg E, Nord DG, Soller M, Lesko N, Wedell A, Bruhn H, Freyer C, Stranneheim H, Wibom R, Nennesmo I, Wredenberg A, Eklund EA, Fellman V. Tegelberg S, et al. Orphanet J Rare Dis. 2017 Apr 20;12(1):73. doi: 10.1186/s13023-017-0624-2. Orphanet J Rare Dis. 2017. PMID: 28427446 Free PMC article.
77 results