Novel mutation in TNPO3 causes congenital limb-girdle myopathy with slow progression

Authors

Anna Vihola, University of Helsinki
Johanna Palmio, Tampere University
Olof Danielsson, Linkoping University
Sini Penttilä, Tampere University
Daniel Louiselle, Washington University School of Medicine in St. Louis
Sara Pittman, Washington University School of Medicine in St. Louis
Conrad Weihl, Washington University School of Medicine in St. Louis
Bjarne Udd, University of Helsinki

Journal

Neurology Genetics

Publication Date

2019

Volume

5

Issue

3

Inclusive Pages

e337

Document Type

Open Access Publication

DOI

10.1212/NXG.0000000000000337

Rights and Permissions

Novel mutation in TNPO3 causes congenital limb-girdle myopathy with slow progression Anna Vihola, Johanna Palmio, Olof Danielsson, Sini Penttilä, Daniel Louiselle, Sara Pittman, Conrad Weihl, Bjarne Udd Neurol Genet Jun 2019, 5 (3) e337; DOI: 10.1212/NXG.0000000000000337 his is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-No Derivatives License 4.0 (CC BY-NC-ND), which permits downloading and sharing the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal.

Recommended Citation

Vihola, Anna; Palmio, Johanna; Danielsson, Olof; Penttilä, Sini; Louiselle, Daniel; Pittman, Sara; Weihl, Conrad; and Udd, Bjarne, "Novel mutation in TNPO3 causes congenital limb-girdle myopathy with slow progression." Neurology Genetics. 5, 3. e337. (2019).
https://digitalcommons.wustl.edu/open_access_pubs/7910