Establishing prevalence in rare neuromuscular diseases: A lesson from congenital myopathies

Authors

Ahmed K. Bamaga, Washington University School of Medicine in St. Louis
Conrad C. Weihl, Washington University School of Medicine in St. Louis

Journal

Neurology: Genetics

Publication Date

2017

Volume

3

Issue

2

Document Type

Open Access Publication

DOI

10.1212/NXG.0000000000000146

Rights and Permissions

Bamaga, A. K., & Weihl, C. C. (2017). Establishing prevalence in rare neuromuscular diseases: A lesson from congenital myopathies. Neurology: Genetics, 3(2) doi:10.1212/NXG.0000000000000146 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives 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

Bamaga, Ahmed K. and Weihl, Conrad C., "Establishing prevalence in rare neuromuscular diseases: A lesson from congenital myopathies." Neurology: Genetics. 3, 2. (2017).
https://digitalcommons.wustl.edu/open_access_pubs/7158