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Human Mutation, ISSN 1059-7794, 04/2015, Volume 36, Issue 4, pp. 395 - 402
Journal Article
Human Molecular Genetics, ISSN 0964-6906, 02/2011, Volume 20, Issue 3, pp. 589 - 600
Prolonged depolarization of skeletal muscle cells induces entry of extracellular calcium into muscle cells, an event referred to as excitation-coupled calcium... 
MUSCLE RYANODINE RECEPTOR | SKELETAL-MUSCLE | RYR1 MUTATIONS | MALIGNANT HYPERTHERMIA | NITRIC-OXIDE SYNTHASE | CALCIUM HOMEOSTASIS | BIOCHEMISTRY & MOLECULAR BIOLOGY | ENDOTHELIAL-CELLS | GENETICS & HEREDITY | SARCOPLASMIC-RETICULUM | COMMON-CAUSE | C2C12 MYOTUBES
Journal Article
Acta Paediatrica, ISSN 0803-5253, 12/2012, Volume 101, Issue 12, pp. 1265 - 1269
Journal Article
American Journal of Medical Genetics Part A, ISSN 1552-4825, 12/2015, Volume 167, Issue 12, pp. 3076 - 3081
Journal Article
by Anderson, Beverley H and Kasher, Paul R and Mayer, Josephine and Szynkiewicz, Marcin and Jenkinson, Emma M and Bhaskar, Sanjeev S and Urquhart, Jill E and Daly, Sarah B and Dickerson, Jonathan E and O'Sullivan, James and Leibundgut, Elisabeth Oppliger and Muter, Joanne and Abdel-Salem, Ghada M. H and Babul-Hirji, Riyana and Baxter, Peter and Berger, Anea and Bonafé, Luisa and Brunstom-Hernandez, Janice E and Buckard, Johannes A and Chitayat, David and Chong, Wui K and Cordelli, Duccio M and Ferreira, Patrick and Fluss, Joel and Forrest, Ewan H and Franzoni, Emilio and Garone, Caterina and Hammans, Simon R and Houge, Gunnar and Hughes, Imelda and Jacquemont, Sebastien and Jeannet, Pierre-Yves and Jefferson, Rosalind J and Kumar, Ram and Kutschke, Georg and Lundberg, Staffan and Lourenço, Charles M and Mehta, Ramesh and Naidu, Sakkubai and Nischal, Ken K and Nunes, Luís and Ounap, Katrin and Philippart, Michel and Prabhakar, Prab and Risen, Sarah R and Schiffmann, Raphael and Soh, Calvin and Stephenson, John B. P and Stewart, Helen and Stone, Jon and Tolmie, John L and van der Knaap, Marjo S and Vieira, Jose P and Vilain, Catheline N and Wakeling, Emma L and Wermenbol, Vanessa and Whitney, Anea and Lovell, Simon C and Meyer, Stefan and Livingston, John H and Baerlocher, Gabriela M and Black, Graeme C. M and Rice, Gillian I and Crow, Yanick J and Medicinska fakulteten and Medicinska och farmaceutiska vetenskapsområdet and Institutionen för kvinnors och barns hälsa and Uppsala universitet
Nature genetics, ISSN 1061-4036, 2012, Volume 44, Issue 3, pp. 338 - 342
Journal Article
Human Mutation, ISSN 1059-7794, 06/2012, Volume 33, Issue 6, pp. 981 - 988
Journal Article
Acta Paediatrica, ISSN 0803-5253, 03/2011, Volume 100, Issue 3, pp. 464 - 466
Journal Article
Annals of Neurology, ISSN 0364-5134, 10/2010, Volume 68, Issue 4, pp. 511 - 520
Journal Article
Revue medicale suisse, ISSN 1660-9379, 02/2012, Volume 8, Issue 329, p. 409
Duchenne muscular dystrophy is an X-linked progressive muscle disease. Since the discovery of the dystrophin gene responsible for the condition, various... 
Genetic Therapy | Muscular Dystrophy, Duchenne - drug therapy | Humans | Muscular Dystrophy, Duchenne - genetics | Child
Journal Article
Journal of Neurology, ISSN 0340-5354, 1/2014, Volume 261, Issue 1, pp. 152 - 163
Journal Article