Dystrophin Genotype–Cardiac Phenotype Correlations in Duchenne and Becker Muscular Dystrophies Using...
Dystrophin Genotype–Cardiac Phenotype Correlations in Duchenne and Becker Muscular Dystrophies Using Cardiac Magnetic Resonance Imaging
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Author / Creator
Tandon, Animesh, MD, MS , Jefferies, John L., MD, MPH , Villa, Chet R., MD , Hor, Kan N., MD , Wong, Brenda L., MD , Ware, Stephanie M., MD, PhD , Gao, Zhiqian, PhD , Towbin, Jeffrey A., MD, MS , Mazur, Wojciech, MD , Fleck, Robert J., MD , Sticka, Joshua J., MD , Benson, D. Woodrow, MD, PhD and Taylor, Michael D., MD, PhD
Publisher
United States: Elsevier Inc
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Language
English
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Publisher
United States: Elsevier Inc
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Scope and Contents
Contents
Duchenne and Becker muscular dystrophies are caused by mutations in dystrophin. Cardiac manifestations vary broadly, making prognosis difficult. Current dystrophin genotype–cardiac phenotype correlations are limited. For skeletal muscle, the reading-frame rule suggests in-frame mutations tend to yield milder phenotypes. We performed dystrophin geno...
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Full title
Dystrophin Genotype–Cardiac Phenotype Correlations in Duchenne and Becker Muscular Dystrophies Using Cardiac Magnetic Resonance Imaging
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Record Identifier
TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_5568575
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_5568575
Other Identifiers
ISSN
0002-9149,1879-1913
E-ISSN
1879-1913
DOI
10.1016/j.amjcard.2015.01.030