Similar articles

• Mutations in dynamin 2 cause dominant centronuclear myopathy.

  Bitoun M, Maugenre S, Jeannet PY, Lacène E, Ferrer X, Laforêt P, Martin JJ, Laporte J, Lochmüller H, Beggs AH, Fardeau M, Eymard B, Romero NB, Guicheney P. Bitoun M, et al. Nat Genet. 2005 Nov;37(11):1207-9. doi: 10.1038/ng1657. Epub 2005 Oct 16. Nat Genet. 2005. PMID: 16227997
• Adult course in dynamin 2 dominant centronuclear myopathy with neonatal onset.

  Melberg A, Kretz C, Kalimo H, Wallgren-Pettersson C, Toussaint A, Böhm J, Stålberg E, Laporte J. Melberg A, et al. Neuromuscul Disord. 2010 Jan;20(1):53-6. doi: 10.1016/j.nmd.2009.10.006. Epub 2009 Nov 22. Neuromuscul Disord. 2010. PMID: 19932619
• Dynamin 2 mutations cause sporadic centronuclear myopathy with neonatal onset.

  Bitoun M, Bevilacqua JA, Prudhon B, Maugenre S, Taratuto AL, Monges S, Lubieniecki F, Cances C, Uro-Coste E, Mayer M, Fardeau M, Romero NB, Guicheney P. Bitoun M, et al. Ann Neurol. 2007 Dec;62(6):666-70. doi: 10.1002/ana.21235. Ann Neurol. 2007. PMID: 17932957
• Structural insights into the centronuclear myopathy-associated functions of BIN1 and dynamin 2.

  Hohendahl A, Roux A, Galli V. Hohendahl A, et al. J Struct Biol. 2016 Oct;196(1):37-47. doi: 10.1016/j.jsb.2016.06.015. Epub 2016 Jun 23. J Struct Biol. 2016. PMID: 27343996 Free PMC article. Review.
• Dynamin 2-related centronuclear myopathy: clinical, histological and genetic aspects of further patients and review of the literature.

  Jeub M, Bitoun M, Guicheney P, Kappes-Horn K, Strach K, Druschky KF, Weis J, Fischer D. Jeub M, et al. Clin Neuropathol. 2008 Nov-Dec;27(6):430-8. doi: 10.5414/npp27430. Clin Neuropathol. 2008. PMID: 19130742 Review.