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Clinical features and genotypes of Laing distal myopathy in a group of Chinese patients, with in-frame deletions of MYH7 as common mutations
Yu M, Zhu Y, Lu Y, et al.
Orphanet journal of rare diseases, 2020, 15, 1, p 344
Molecular landscape of CAPN3 mutations in limb-girdle muscular dystrophy type R1: from a Chinese multicentre analysis to a worldwide perspective
Zhong H, Zheng Y, Zhao Z, et al.
Journal of medical genetics, 2020
Expansion of GGC Repeat in GIPC1 Is Associated with Oculopharyngodistal Myopathy
Deng J, Yu J, Li P, et al.
American journal of human genetics, 2020, 106, 6, p 793
Mutational and clinical spectrum in a cohort of Chinese patients with hereditary nemaline myopathy
Wang Q, Hu Z, Chang X, et al.
Clinical genetics, 2020
Value of muscle magnetic resonance imaging in the differential diagnosis of muscular dystrophies related to the dystrophin-glycoprotein complex
Xie Z, Xie Z, Yu M, et al.
Orphanet journal of rare diseases, 2019, 14, 1, p 250
Clinical and genetic spectrum of sarcoglycanopathies in a large cohort of Chinese patients
Xie Z, Xie Z, Hou Y, et al.
Orphanet journal of rare diseases, 2019, 14, 1
Mutational spectrum of Chinese LGMD patients by targeted next-generation sequencing
Yu M, Zheng Y, Jin S, et al.
PLoS ONE, 2017, 12, 4
Adeno-associated viral mediated LARGE gene therapy rescues the muscular dystrophic phenotype in mouse models of dystroglycanopathy
Yu M, He Y, Wang K, et al.
Human gene therapy, 2013, 24, 3, p. 317-330
Enhanced effect of microdystrophin gene transfection by HSV-VP22 mediated intercellular protein transport
Xiong F, Xiao S, Yu M, et al.
BioMed Central neuroscience, 2007, 8, 50, p. 1-9
BM stem cell transplantation rescues pathophysiologic features of aged dystrophic mdx muscle
Yu M, Zhang C, Zhang Y, et al.
Cytotherapy, 2007, 9, 1, p. 44-52
Increased titer of recombinant AAV vectors by gene transfer with adenovirus coupled to DNA-polylysine complexes
Mamounas M, Leavitt M, Yu M, et al.
Gene therapy, 1995, 2, p. 429-432
