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

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

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.

Flanigan KM; Center for Gene Therapy, Nationwide Children's Hospital, Columbus, Ohio, USA. kevin.flanigan@nationwidechildrens.org

Hum Mutat ; 32(3): 299-308, 2011 Mar.

Article en En | MEDLINE | ID: mdl-21972111

Asunto(s)

Codón sin Sentido; Distrofina/genética; Exones; Distrofia Muscular de Duchenne/genética; Empalme del ARN; Femenino; Humanos; Masculino; Distrofia Muscular de Duchenne/metabolismo; Fenotipo; Empalme del ARN/genética

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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Empalme del ARN / Exones / Distrofina / Codón sin Sentido / Distrofia Muscular de Duchenne Tipo de estudio: Prognostic_studies / Risk_factors_studies Límite: Female / Humans / Male Idioma: En Año: 2011 Tipo del documento: Article

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