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2011 2
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2015 1
2017 1
2018 1
2020 2
2021 1
2023 0
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Page 1
Structure of the F-actin-tropomyosin complex.
von der Ecken J, Müller M, Lehman W, Manstein DJ, Penczek PA, Raunser S. von der Ecken J, et al. Nature. 2015 Mar 5;519(7541):114-7. doi: 10.1038/nature14033. Epub 2014 Dec 1. Nature. 2015. PMID: 25470062 Free PMC article.
Novel ACTA1 mutation causes late-presenting nemaline myopathy with unusual dark cores.
Garibaldi M, Fattori F, Pennisi EM, Merlonghi G, Fionda L, Vanoli F, Leonardi L, Bucci E, Morino S, Micaloni A, Tartaglione T, Uijterwijk B, Zierikzee M, Ottenheijm C, Bertini ES, Stoppacciaro A, Raffa S, Salvetti M, Antonini G. Garibaldi M, et al. Neuromuscul Disord. 2021 Feb;31(2):139-148. doi: 10.1016/j.nmd.2020.11.012. Epub 2020 Nov 30. Neuromuscul Disord. 2021. PMID: 33384202
Protein aggregation in congenital myopathies.
Goebel HH, Blaschek A. Goebel HH, et al. Semin Pediatr Neurol. 2011 Dec;18(4):272-6. doi: 10.1016/j.spen.2011.10.009. Semin Pediatr Neurol. 2011. PMID: 22172423 Review.