Characterization of translational frame exception patients in Duchenne/Becker muscular dystrophy

The clinical progression of Duchenne muscular dystrophy (DMD) patients with deletions can be predicted in 93% of cases by whether the deletion maintains or disrupts the translational reading frame (frameshift hypothesis). We have identified and studied a number of patients who have deletions that do...

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Veröffentlicht in:Human molecular genetics 1993-06, Vol.2 (6), p.737-744
Hauptverfasser: Winnard, Alissa V., Klein, Christopher J., Coovert, Daniel D., Prior, Thomas, Papp, Audrey, Snyder, Pamela, Bulman, Dennis E., Ray, Peter N., McAndrew, Patricia, King, Wendy, Moxley, Richard T., Mendell, Jerry R., Burghes, Arthur H.M.
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Sprache:eng
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