Intron mutations and early transcription termination in Duchenne and Becker muscular dystrophy

Waldrop, M. A., Moore, S. A., Mathews, K. D., Darbro, B. W., Medne, L., Finkel, R., Connolly, A. M., Crawford, T. O., Drachman, D., Wein, N., Habib, A. A., Krzesniak‐Swinarska, M. A., Zaidman, C. M., Collins, J. J., Jokela, M., Udd, B., Day, J. W., Ortiz‐Guerrero, G., Statland, J., … Flanigan, K. M. (2022). Intron mutations and early transcription termination in Duchenne and Becker muscular dystrophy. Human Mutation, 43(4), 511–528. Portico. https://doi.org/10.1002/humu.24343
Authors:
Megan A. Waldrop
Nicolas Wein
Kevin M. Flanigan
Steven A. Moore
Katherine D. Mathews
Benjamin W. Darbro
Livja Medne
Richard Finkel
Anne M. Connolly
Craig M. Zaidman
Thomas O. Crawford
Daniel Drachman
Ali A. Habib
Monika A. Krzesniak-Swinarska
James J. Collins
Manu Jokela
Bjarne Udd
John W. Day
Gloria Ortiz-Guerrero
Jeff Statland
Russell J. Butterfield
Robert B. Weiss
Diane M. Dunn
Affiliated Authors:
Ali A. Habib
Author Keywords:
becker muscular dystrophy
deep intronic
duchenne muscular dystrophy
pseudoexon
telescripting
transcription termination
Publication Type:
Article
Unique ID:
10.1002/humu.24343
PMID:
Journal:
Publication Date:
Data Source:
Web of Science

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