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

Year of publication

2022

Authors

Waldrop, Megan A.; Moore, Steven A.; Mathews, Katherine D.; Darbro, Benjamin W.; Medne, Livja; Finkel, Richard; Connolly, Anne M.; Crawford, Thomas O.; Drachman, Daniel; Wein, Nicolas; Habib, Ali A.; Krzesniak-Swinarska, Monika A.; Zaidman, Craig M.; Collins, James J.; Jokela, Manu; Udd, Bjarne; Day, John W.; Ortiz-Guerrero, Gloria; Statland, Jeff; Butterfield, Russell J.; Dunn, Diane M.; Weiss, Robert B.; Flanigan, Kevin M.
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Organizations and authors

Tampere University

Udd Bjarne

Jokela Manu

University of Turku

Jokela Manu

Tampere University Hospital

Udd Bjarne

Jokela Manu

Turku University Central Hospital

Jokela Manu

Publication type

Publication format

Article

Parent publication type

Journal

Article type

Original article

Audience

Scientific

Peer-reviewed

Peer-Reviewed

MINEDU's publication type classification code

A1 Journal article (refereed), original research

Publication channel information

Journal/Series

Human mutation

Volume

43

Issue

4

Pages

511-528

ISSN

1059-7794

​Publication forum

57255

​Publication forum level

2

Open access

Open access in the publisher’s service

No

Open access of publication channel

Partially open publication channel

Self-archived

No

Other information

Fields of science

Genetics, developmental biology, physiology; Neurosciences; Neurology and psychiatry

Identified topic

[object Object]

Internationality of the publisher

International

Language

English

International co-publication

Yes

Co-publication with a company

Yes

DOI

10.1002/humu.24343

The publication is included in the Ministry of Education and Culture’s Publication data collection

Yes