The DOI matches its Crossref record; 2 of the 2 references it cites were found in a registry or an index.
Molecular basis of Thomsen's disease (autosomal dominant myotonia congenita)
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Citations
Cites
Calcium channel characteristics conferred on the sodium channel by single mutations
Heinemann, S. H., Terlau, H., Stühmer, W., Imoto, K., & Numa, S. (1992) · Nature · doi:10.1038/356441a0 · Cited by 784
Rosenfeld, P. J., Cowley, G. S., McGee, T. L., Sandberg, M. A., Berson, E. L., & Dryja, T. P. (1992) · Nature Genetics · doi:10.1038/ng0692-209 · Cited by 422
Cited by
Molecular Structure and Physiological Function of Chloride Channels
Jentsch, T. J., Stein, V., Weinreich, F., & Zdebik, A. A. (2002) · Physiological Reviews · doi:10.1152/physrev.00029.2001 · Cited by 1,256
Calcium-activated potassium channels
Vergara, C., Latorre, R., Marrion, N. V., & Adelman, J. P. (1998) · Current Opinion in Neurobiology · doi:10.1016/s0959-4388(98)80056-1 · Cited by 954
Structure of the CLC-1 chloride channel from Homo sapiens
Park, E., & MacKinnon, R. (2018) · eLife · doi:10.7554/elife.36629 · Cited by 109
The familial periodic paralyses and nondystrophic myotonias
Ptáček, L. (1998) · The American Journal of Medicine · doi:10.1016/s0002-9343(98)00123-5 · Cited by 82
Maggi, L., Bonanno, S., Altamura, C., & Desaphy, J.-F. (2021) · Cells · doi:10.3390/cells10061521 · Cited by 51
Metadata
- Authors
- George, A. L., Crackower, M. A., Abdalla, J. A., Hudson, A. J., & Ebers, G. C.
- Venue
- Nature Genetics
- Published
- 1993-04
- Volume
- 3
- Issue
- 4
- Pages
- 305-310
- ISSN
- 1061-4036 (ISSN-L)
- 1546-1718
- OpenAlex
- W2086734513
- Cited by
- 283
- References
- 2
- FWCI
- 7.87
- Type
- journal article
- Language
- en
- Open access
- closed
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- CoChat. (2026). Citation check: Molecular basis of Thomsen's disease (autosomal dominant myotonia congenita). https://app.cochat.ai/papers/10.1038/ng0493-305
- The paper
- George, A. L., Crackower, M. A., Abdalla, J. A., Hudson, A. J., & Ebers, G. C. (1993). Molecular basis of Thomsen's disease (autosomal dominant myotonia congenita). Nature Genetics. https://doi.org/10.1038/ng0493-305
Data sources
Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.
