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Genetic characterization in symptomatic female DMD carriers: lack of relationship between X-inactivation, transcriptional DMD allele balancing and phenotype.
- Published in:
- BMC Medical Genetics, 2012, v. 13, n. 1, p. 73, doi. 10.1186/1471-2350-13-73
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- Article
Corrigendum: Translation from a DMD exon 5 IRES results in a functional dystrophin isoform that attenuates dystrophinopathy in humans and mice.
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- Nature Medicine, 2015, v. 21, n. 5, p. 537, doi. 10.1038/nm0515-537c
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- Publication type:
- Article
Corrigendum: Translation from a DMD exon 5 IRES results in a functional dystrophin isoform that attenuates dystrophinopathy in humans and mice.
- Published in:
- Nature Medicine, 2015, v. 21, n. 4, p. 414, doi. 10.1038/nm0415-414b
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- Publication type:
- Article
Translation from a DMD exon 5 IRES results in a functional dystrophin isoform that attenuates dystrophinopathy in humans and mice.
- Published in:
- Nature Medicine, 2014, v. 20, n. 9, p. 992, doi. 10.1038/nm.3628
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- Article