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Year | Number of Results |
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2004 | 1 |
2021 | 2 |
2024 | 0 |
PubMed (cited) for id: 619219
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Loss of C2orf69 defines a fatal autoinflammatory syndrome in humans and zebrafish that evokes a glycogen-storage-associated mitochondriopathy.
Am J Hum Genet. 2021 Jul 1;108(7):1301-1317. doi: 10.1016/j.ajhg.2021.05.003. Epub 2021 May 25.
Am J Hum Genet. 2021.
PMID: 34038740
Free PMC article.
C2orf69 mutations disrupt mitochondrial function and cause a multisystem human disorder with recurring autoinflammation.
Lausberg E, Gießelmann S, Dewulf JP, Wiame E, Holz A, Salvarinova R, van Karnebeek CD, Klemm P, Ohl K, Mull M, Braunschweig T, Weis J, Sommer CJ, Demuth S, Haase C, Stollbrink-Peschgens C, Debray FG, Libioulle C, Choukair D, Oommen PT, Borkhardt A, Surowy H, Wieczorek D, Wagner N, Meyer R, Eggermann T, Begemann M, Van Schaftingen E, Häusler M, Tenbrock K, van den Heuvel L, Elbracht M, Kurth I, Kraft F.
Lausberg E, et al.
J Clin Invest. 2021 Jun 15;131(12):e143078. doi: 10.1172/JCI143078.
J Clin Invest. 2021.
PMID: 33945503
Free PMC article.
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Large-scale gene expression analysis of human skeletal myoblast differentiation.
Sterrenburg E, Turk R, 't Hoen PA, van Deutekom JC, Boer JM, van Ommen GJ, den Dunnen JT.
Sterrenburg E, et al.
Neuromuscul Disord. 2004 Sep;14(8-9):507-18. doi: 10.1016/j.nmd.2004.03.008.
Neuromuscul Disord. 2004.
PMID: 15336692
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