Cracking the code: Genotype-phenotype correlation models in sarcoglycanopathies

Authors

• Leonela Luce, Newcastle University
• Conrad C Weihl, Washington University School of Medicine in St. Louis
• et al.

Journal

Annals of Clinical and Translational Neurology

Publication Date

9-1-2026

Volume

13

Issue

9

First Page

1851

Last Page

1865

Document Type

Open Access Publication

DOI

10.1002/acn3.70361

Rights and Permissions

L. Luce, G. S. Kocak, J. Verdú-Díaz, et al., “ Cracking the Code: Genotype–Phenotype Correlation Models in Sarcoglycanopathies,” Annals of Clinical and Translational Neurology 13, no. 9 (2026): 1851–1865, https://doi.org/10.1002/acn3.70361. © 2026 The Author(s). Annals of Clinical and Translational Neurology published by Wiley Periodicals LLC on behalf of American Neurological Association. This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.

Recommended Citation

Luce, Leonela; Weihl, Conrad C; and et al., "Cracking the code: Genotype-phenotype correlation models in sarcoglycanopathies." Annals of Clinical and Translational Neurology. 13, 9. 1851 - 1865. (2026).
https://digitalcommons.wustl.edu/oa_4/7269

Department

ICTS (Institute of Clinical and Translational Sciences)

Additional Links

Supplemental material is available for this article at publisher site.