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Gentamicin-induced readthrough of stop codons in duchenne muscular dystrophy

✍ Scribed by Vinod Malik; Louise R. Rodino-Klapac; Laurence Viollet; Cheryl Wall; Wendy King; Roula Al-Dahhak; Sarah Lewis; Christopher J. Shilling; Janaiah Kota; Carmen Serrano-Munuera; John Hayes; John D. Mahan; Katherine J. Campbell; Brenda Banwell; Majed Dasouki; Victoria Watts; Kumaraswamy Sivakumar; Ricardo Bien-Willner; Kevin M. Flanigan; Zarife Sahenk; Richard J. Barohn; Christopher M. Walker; Jerry R. Mendell

Publisher
John Wiley and Sons
Year
2010
Tongue
English
Weight
266 KB
Volume
67
Category
Article
ISSN
0364-5134

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## Abstract ## Background The most common form of congenital muscular dystrophy is caused by a deficiency in the Ξ±2 chain of laminin‐211, a protein of the extracellular matrix. A wide variety of mutations, including 20 to 30% of nonsense mutations, have been identified in the corresponding gene, _