Dystrophin in frameshift deletion patients with Becker muscular dystrophy.

In a previous study we identified 14 cases with Duchenne muscular dystrophy (DMD) or its milder variant, Becker muscular dystrophy (BMD), with a deletion of exons 3-7, a deletion that would be expected to shift the translational reading frame of the mRNA and give a severe phenotype. We have examined...

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Bibliografiset tiedot
Päätekijät: Gangopadhyay, S B, Sherratt, T G, Heckmatt, J Z, Dubowitz, V, Miller, G, Shokeir, M, Ray, P N, Strong, P N, Worton, R G
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: 1992
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Research Article
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC1682710/
https://ncbi.nlm.nih.gov/pubmed/1496988
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