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Ataluren in patients with nonsense mutation Duchenne musc... | ResearchHub
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Ataluren in patients with nonsense mutation Duchenne muscular dystrophy (ACT DMD): a multicentre, randomised, double-blind, placebo-controlled, phase 3 trial
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Authors
Craig McDonald
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Craig McDonald
•
Craig Campbell
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•
Giuseppe Vita
Published
July 17, 2017
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Journal
The Lancet
Topics
Chemistry
Biochemistry
Medicine
Pathology
Internal Medicine
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DOI
10.1016/s0140-6736(17)31611-2
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Supporters
Support the authors with ResearchCoin
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Journal
The Lancet
Topics
Chemistry
Biochemistry
Medicine
Pathology
Internal Medicine
Show all topics
DOI
10.1016/s0140-6736(17)31611-2
Other Formats
PDF
