original ) (raw )Becker muscular dystrophy with marked divergence between clinical and molecular genetic findings: case series
Joachim Weis
Swiss medical weekly, 2006
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A rare subclinical or mild type of Becker muscular dystrophy caused by a single exon 48 deletion of the dystrophin gene
Jacek Pilch
Journal of Applied Genetics, 2017
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A 400-kb tandem duplication within the dystrophin gene leads to severe Becker muscular dystrophy
Wolfram Kress
Journal of Neurology, 1994
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C-Terminal Truncated Dystrophin Identified in Skeletal Muscle of an Asymptomatic Boy with a Novel Nonsense Mutation of the Dystrophin Gene
Masafumi Matsuo
Pediatric Research, 2004
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Mutation Spectrum of Dystrophin Gene in Malaysian Patients with Duchenne/Becker Muscular Dystrophy
David Bunyan
Journal of Neurogenetics, 2013
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Characterization of genetic deletions in becker muscular dystrophy using monoclonal antibodies against a deletion-prone region of dystrophin
Caroline Sewry
American Journal of Medical Genetics, 1995
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Up-Regulation of the Brain and Purkinje-Cell Forms of Dystrophin Transcripts, in Becker Muscular Dystrophy
Shin'Ichi Takeda
The American Journal of Human Genetics, 1997
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Analysis of dystrophin gene in Iranian Duchenne and Becker muscular dystrophies patients and identification of a novel mutation
Gholamreza Zamani
Neurological Sciences, 2015
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Relatively low proportion of dystrophin gene deletions in Israeili Duchenne and Becker muscular dystrophy patients
ruth shomrat
Amer J Med Genet, 1994
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Patterns of dystrophin gene deletion in Egyptian Duchenne/Becker muscular dystrophy patients
nagia fahmy
Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology / edited by the Gaetano Conte Academy for the study of striated muscle diseases, 2007
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Dystrophin and the two related genetic diseases, Duchenne and Becker muscular dystrophies
BJBMS Journal
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Very small dystrophin molecule in a family with a mild form of Becker dystrophy
Renato Mantegazza
Neuromuscular Disorders, 1993
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Functional changes in Becker muscular dystrophy: implications for clinical trials in dystrophinopathies OPEN
Corrado I Angelini
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Deletion mutations in the dystrophin gene of Saudi patients with Duchenne and Becker muscular dystrophy
adnan awada
Saudi medical journal, 2002
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Molecular analysis of Duchenne/Becker muscular dystrophy
Giulia Frisso
Frontiers in Bioscience, 2010
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Clinicopathologic and molecular profiles of Duchenne and Becker muscular dystrophy
Putri Insani
Paediatrica Indonesiana, 2019
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Analysis of Scottish Duchenne and Becker muscular dystrophy families with dystrophin cDNA probes
Douglas Wilcox
Journal of Medical Genetics, 1990
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Mutation spectrum of the dystrophin gene in 442 Duchenne/Becker muscular dystrophy cases from one Japanese referral center
Masafumi Matsuo
Journal of Human Genetics, 2010
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Deletion patterns of dystrophin gene in Hungarian patients with Duchenne/Becker muscular dystrophies
István Raskó , E. Morava
Neuromuscular Disorders, 1999
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Becker muscular dystrophy severity is linked to the structure of dystrophin
Sylvie Tuffery-giraud
Human Molecular Genetics, 2014
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Duchenne and Becker muscular dystrophy: a molecular and immunohistochemical approach
Lineu Werneck
Arquivos de Neuro-Psiquiatria, 2007
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DGGE-based whole-gene mutation scanning of the dystrophin gene in Duchenne and Becker muscular dystrophy patients
Ieke Ginjaar
Human Mutation, 2003
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Tandem duplications of two separate fragments of the dystrophin gene in a patient with Duchenne muscular dystrophy
Van Tran
Journal of Human Genetics, 2008
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Double missense mutation in exon 41 of the human dystrophin gene detected by double strand conformation analysis
Luciano Merlini
American Journal of Medical Genetics, 1998
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Genetic Profile of the Dystrophin Gene Reveals New Mutations in Colombian Patients Affected with Muscular Dystrophinopathy
Natalia Morales Fonseca
The Application of Clinical Genetics, 2021
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Analyses of the presence of mutations in Dystrophin protein to predict their relative influences in the onset of Duchenne Muscular Dystrophy
Angshuman Bagchi
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