Becker muscular dystrophy: case report, review of the literature, and analysis of differentially expressed hub genes

[11] Goshima N(2011)Study of dystrophin gene non-deletion/duplication mutations causing Becker muscular dystrophy Zhonghua Yi Xue Yi Chuan Xue Za Zhi 53 439-441

[12] Ueno M(2015)Novel rod domain duplication in dystrophin resulting in X-linked dilated cardiomyopathy Pediatr Neurol 20 61-63

[13] Bushby K(2010)Coinheritance of Noonan syndrome and Becker muscular dystrophy Neuromuscul Disord 39 239-243

[14] Finkel R(2009)Asymptomatic Becker muscular dystrophy in a family with a multiexon deletion Muscle Nerve 37 702-705

[15] Birnkrant DJ(2012)Beneficial effect of ivabradine in dilated cardiomyopathy from Becker muscular dystrophy Herz 44 822-825

[16] Case LE(2011)Becker muscular dystrophy due to an inversion of exons 23 and 24 of the DMD gene Muscle Nerve 149A 1052-1055

[17] Clemens PR(2009)Homozygous female Becker muscular dystrophy Am J Med Genet A 30 e1-956.e3

[18] Cripe L(2014)A novel dystrophin deletion mutation in a Becker muscular dystrophy patient with early-onset dilated cardiomyopathy Can J Cardiol 63 81-89

[19] El-Aloul B(2008)DMD pseudoexon mutations: splicing efficiency, phenotype, and potential therapy Ann Neurol 52 459-460

[20] Altamirano-Diaz L(2014)Prenatal diagnosis of BMD in Morocco: evolution and limits J Mol Neurosci 20 251-254

[11] Goshima N(2011)Study of dystrophin gene non-deletion/duplication mutations causing Becker muscular dystrophy Zhonghua Yi Xue Yi Chuan Xue Za Zhi 53 439-441

[12] Ueno M(2015)Novel rod domain duplication in dystrophin resulting in X-linked dilated cardiomyopathy Pediatr Neurol 20 61-63

[13] Bushby K(2010)Coinheritance of Noonan syndrome and Becker muscular dystrophy Neuromuscul Disord 39 239-243

[14] Finkel R(2009)Asymptomatic Becker muscular dystrophy in a family with a multiexon deletion Muscle Nerve 37 702-705

[15] Birnkrant DJ(2012)Beneficial effect of ivabradine in dilated cardiomyopathy from Becker muscular dystrophy Herz 44 822-825

[16] Case LE(2011)Becker muscular dystrophy due to an inversion of exons 23 and 24 of the DMD gene Muscle Nerve 149A 1052-1055

[17] Clemens PR(2009)Homozygous female Becker muscular dystrophy Am J Med Genet A 30 e1-956.e3

[18] Cripe L(2014)A novel dystrophin deletion mutation in a Becker muscular dystrophy patient with early-onset dilated cardiomyopathy Can J Cardiol 63 81-89

[19] El-Aloul B(2008)DMD pseudoexon mutations: splicing efficiency, phenotype, and potential therapy Ann Neurol 52 459-460

[20] Altamirano-Diaz L(2014)Prenatal diagnosis of BMD in Morocco: evolution and limits J Mol Neurosci 20 251-254