Nonsense mutation-associated Becker muscular dystrophy: interplay between exon definition and splicing regulatory elements within the DMD gene-Reference-Cited by-同舟云学术

Nonsense mutation-associated Becker muscular dystrophy: interplay between exon definition and splicing regulatory elements within the DMD gene

Published:2011-02-22 Issue:3 Volume:32 Page:299-308
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Hum. Mutat.

Author:

Flanigan Kevin M.,Dunn Diane M.,von Niederhausern Andrew,Soltanzadeh Payam,Howard Michael T.,Sampson Jacinda B.,Swoboda Kathryn J.,Bromberg Mark B.,Mendell Jerry R.,Taylor Laura E.,Anderson Christine B.,Pestronk Alan,Florence Julaine M.,Connolly Anne M.,Mathews Katherine D.,Wong Brenda,Finkel Richard S.,Bonnemann Carsten G.,Day John W.,McDonald Craig,Weiss Robert B.,

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/humu.21426/fullpdf

Reference54 articles.

1. Antisense-mediated exon skipping: a versatile tool with therapeutic and research applications;Aartsma-Rus;RNA,2007

2. Deciphering the splicing code;Barash;Nature,2010

3. Computational analysis of candidate intron regulatory elements for tissue-specific alternative pre-mRNA splicing;Brudno;Nucleic Acids Res,2001

4. Disruption of an SF2/ASF-dependent exonic splicing enhancer in SMN2 causes spinal muscular atrophy in the absence of SMN1;Cartegni;Nat Genet,2002

5. Improved molecular diagnosis of dystrophinopathies in an unselected clinical cohort;Dent;Am J Med Genet A,2005

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