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Bushby K, Finkel R, Birnkrant DJ, Case LE, Clemens PR, Cripe L, et al. (January 2010). "Diagnosis and management of Duchenne muscular dystrophy, part 1: diagnosis, and pharmacological and psychosocial management". The Lancet. Neurology. 9 (1): 77–93. CiteSeerX10.1.1.176.4466. doi:10.1016/s1474-4422(09)70271-6. PMID19945913. S2CID328499.
Dany A, Barbe C, Rapin A, Réveillère C, Hardouin JB, Morrone I, et al. (November 2015). "Construction of a Quality of Life Questionnaire for slowly progressive neuromuscular disease". Quality of Life Research. 24 (11): 2615–2623. doi:10.1007/s11136-015-1013-8. PMID26141500. S2CID25834947.
Allen DG, Gervasio OL, Yeung EW, Whitehead NP (February 2010). "Calcium and the damage pathways in muscular dystrophy". Canadian Journal of Physiology and Pharmacology. 88 (2): 83–91. doi:10.1139/Y09-058. PMID20237582.
England SB, Nicholson LV, Johnson MA, Forrest SM, Love DR, Zubrzycka-Gaarn EE, et al. (January 1990). "Very mild muscular dystrophy associated with the deletion of 46% of dystrophin". Nature. 343 (6254): 180–182. Bibcode:1990Natur.343..180E. doi:10.1038/343180a0. PMID2404210. S2CID4349360.
Patmanathan SN, Gnanasegaran N, Lim MN, Husaini R, Fakiruddin KS, Zakaria Z (2018). "CRISPR/Cas9 in Stem Cell Research: Current Application and Future Perspective". Current Stem Cell Research & Therapy. 13 (8): 632–644. doi:10.2174/1574888X13666180613081443. PMID29895256. S2CID48357156.
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Bushby K, Finkel R, Birnkrant DJ, Case LE, Clemens PR, Cripe L, et al. (January 2010). "Diagnosis and management of Duchenne muscular dystrophy, part 1: diagnosis, and pharmacological and psychosocial management". The Lancet. Neurology. 9 (1): 77–93. CiteSeerX10.1.1.176.4466. doi:10.1016/s1474-4422(09)70271-6. PMID19945913. S2CID328499.
Sutherland DH, Olshen R, Cooper L, Wyatt M, Leach J, Mubarak S, et al. (February 1981). "The pathomechanics of gait in Duchenne muscular dystrophy". Developmental Medicine and Child Neurology. 23 (1): 3–22. doi:10.1111/j.1469-8749.1981.tb08442.x. PMID7202868. S2CID895379.
Bushby K, Finkel R, Birnkrant DJ, Case LE, Clemens PR, Cripe L, et al. (January 2010). "Diagnosis and management of Duchenne muscular dystrophy, part 1: diagnosis, and pharmacological and psychosocial management". The Lancet. Neurology. 9 (1): 77–93. CiteSeerX10.1.1.176.4466. doi:10.1016/s1474-4422(09)70271-6. PMID19945913. S2CID328499.
Dany A, Barbe C, Rapin A, Réveillère C, Hardouin JB, Morrone I, et al. (November 2015). "Construction of a Quality of Life Questionnaire for slowly progressive neuromuscular disease". Quality of Life Research. 24 (11): 2615–2623. doi:10.1007/s11136-015-1013-8. PMID26141500. S2CID25834947.
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England SB, Nicholson LV, Johnson MA, Forrest SM, Love DR, Zubrzycka-Gaarn EE, et al. (January 1990). "Very mild muscular dystrophy associated with the deletion of 46% of dystrophin". Nature. 343 (6254): 180–182. Bibcode:1990Natur.343..180E. doi:10.1038/343180a0. PMID2404210. S2CID4349360.
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Patmanathan SN, Gnanasegaran N, Lim MN, Husaini R, Fakiruddin KS, Zakaria Z (2018). "CRISPR/Cas9 in Stem Cell Research: Current Application and Future Perspective". Current Stem Cell Research & Therapy. 13 (8): 632–644. doi:10.2174/1574888X13666180613081443. PMID29895256. S2CID48357156.
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"Duchenne muscular dystrophy". Genetic and Rare Diseases (GARD) Information Center. Archived from the original on 23 November 2016. Retrieved 24 January 2021. This article incorporates text from this source, which is in the public domain.
De Rosa G (October 2005). "Da Conte a Duchenne" [By Conte in Duchenne]. DM (in Italian). Unione Italiana Lotta alla Distrofia Muscolare. Archived from the original on 4 March 2016. Retrieved 24 August 2015.
The GearShifters Team (13 September 2022). "How Did Dino Ferrari Die?". GearShifters. Archived from the original on 31 August 2023. Retrieved 31 August 2023.