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Neuromuscular Disorders : NMD|September 25, 2021
Recent advances in nemaline myopathyJenni Laitila, Carina Wallgren-PetterssonEuropean Journal of Human Genetics : EJHG|July 23, 2015
A recurrent copy number variation of the NEB triplicate region: only revealed by the targeted nemaline myopathy CGH arrayKirsi Kiiski, Vilma-Lotta Lehtokari, Ari Löytynoja, et al.Muscle & Nerve|September 29, 2018
A nebulin super-repeat panel reveals stronger actin binding toward the ends of the super-repeat regionJenni Laitila, Johanna Lehtonen, Vilma-Lotta Lehtokari, et al.Skeletal Muscle|August 12, 2014
Nebulin interactions with actin and tropomyosin are altered by disease-causing mutationsMinttu Marttila, Mubashir Hanif, Elina Lemola, et al.Seminars in Pediatric Neurology|July 26, 2002
Nemaline and myotubular myopathiesCarina Wallgren-PetterssonScientific Reports|October 26, 2018
Two alternatively-spliced human nebulin isoforms with either exon 143 or exon 144 and their developmental regulationLe Thanh Lam, Ian Holt, Jenni Laitila, et al.Seminars in Pediatric Neurology|May 8, 2019
Update on the Genetics of Congenital MyopathiesKatarina Pelin, Carina Wallgren-PetterssonAdvances in Experimental Medicine and Biology|February 3, 2009
Nebulin--a giant chameleonKatarina Pelin, Carina Wallgren-PetterssonSeminars in Pediatric Neurology|May 8, 2019
Pregnancy and Delivery in Women With Congenital MyopathiesSabine Rudnik-Schöneborn, Carina Wallgren-PetterssonJournal of Community Genetics|June 28, 2018
Ethics in genetic counsellingAngus J Clarke, Carina Wallgren-PetterssonPageof 10