Pathomechanisms of a CLCN1 Mutation Found in a Russian Family Suffering From Becker's Myotonia
- DOI
- 10.3389/fneur.2020.01019
- Published
- 2020-09-04
- Container
- Frontiers in Neurology
- Publisher
- Frontiers Media SA
- Open access
- unknown
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Cite this work
BibTeX
@article{allodium:10.3389/fneur.2020.01019,
title = {Pathomechanisms of a CLCN1 Mutation Found in a Russian Family Suffering From Becker's Myotonia},
author = {Concetta Altamura and Evgeniya A. Ivanova and Paola Imbrici and Elena Conte and Giulia Maria Camerino and Elena L. Dadali and Alexander V. Polyakov and Sergei Aleksandrovich Kurbatov and Francesco Girolamo and Maria Rosaria Carratù and Jean-François Desaphy},
year = {2020},
journal = {Frontiers in Neurology},
doi = {10.3389/fneur.2020.01019},
url = {https://doi.org/10.3389/fneur.2020.01019}
}RIS
TY - JOUR TI - Pathomechanisms of a CLCN1 Mutation Found in a Russian Family Suffering From Becker's Myotonia AU - Concetta Altamura AU - Evgeniya A. Ivanova AU - Paola Imbrici AU - Elena Conte AU - Giulia Maria Camerino AU - Elena L. Dadali AU - Alexander V. Polyakov AU - Sergei Aleksandrovich Kurbatov AU - Francesco Girolamo AU - Maria Rosaria Carratù AU - Jean-François Desaphy PY - 2020 JO - Frontiers in Neurology DO - 10.3389/fneur.2020.01019 UR - https://doi.org/10.3389/fneur.2020.01019 ER -
APA
Altamura, C., Ivanova, E. A., Imbrici, P., Conte, E., Camerino, G. M., Dadali, E. L., Polyakov, A. V., Kurbatov, S. A., Girolamo, F., Carratù, M. R., & Desaphy, J. (2020). Pathomechanisms of a CLCN1 Mutation Found in a Russian Family Suffering From Becker's Myotonia. Frontiers in Neurology. https://doi.org/10.3389/fneur.2020.01019
Source records
- crossref · retrieved 2026-09-27T02:01:01.244Z