APA

Flanigan K. M., Dunn D. M., von Niederhausern A., Soltanzadeh P., Howard M. T., Sampson J. B., Swoboda K. J., Bromberg M. B., Mendell J. R., Taylor L. E., Anderson C. B., Pestronk A., Florence J. M., Connolly A. M., Mathews K. D., Wong B., Finkel R. S., Bonnemann C. G., Day J. W., McDonald C. & Weiss R. B. (20120327). Nonsense mutation-associated Becker muscular dystrophy: interplay between exon definition and splicing regulatory elements within the DMD gene. : Human mutation.

Chicago

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 and Weiss Robert B. 20120327. Nonsense mutation-associated Becker muscular dystrophy: interplay between exon definition and splicing regulatory elements within the DMD gene. : Human mutation.

Harvard

Flanigan K. M., Dunn D. M., von Niederhausern A., Soltanzadeh P., Howard M. T., Sampson J. B., Swoboda K. J., Bromberg M. B., Mendell J. R., Taylor L. E., Anderson C. B., Pestronk A., Florence J. M., Connolly A. M., Mathews K. D., Wong B., Finkel R. S., Bonnemann C. G., Day J. W., McDonald C. and Weiss R. B. (20120327). Nonsense mutation-associated Becker muscular dystrophy: interplay between exon definition and splicing regulatory elements within the DMD gene. : Human mutation.

MLA

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 and Weiss Robert B. Nonsense mutation-associated Becker muscular dystrophy: interplay between exon definition and splicing regulatory elements within the DMD gene. : Human mutation. 20120327.