The DOI matches its Crossref record.
Mutations in the β-tropomyosin (TPM2) gene – a rare cause of nemaline myopathy
Overview
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Citations
Cited by
Tropomyosin-Based Regulation of the Actin Cytoskeleton in Time and Space
Gunning, P., O’neill, G., & Hardeman, E. (2008) · Physiological Reviews · doi:10.1152/physrev.00001.2007 · Cited by 478
KLHL40 deficiency destabilizes thin filament proteins and promotes nemaline myopathy
Garg, A., O’Rourke, J., Long, C., Doering, J., Ravenscroft, G., Bezprozvannaya, S., Nelson, B. R., Beetz, N., Li, L., Chen, S., et al. (2014) · Journal of Clinical Investigation · doi:10.1172/jci74994 · Cited by 127
Targeting the sarcomere to correct muscle function
Hwang, P. M., & Sykes, B. D. (2015) · Nature Reviews Drug Discovery · doi:10.1038/nrd4554 · Cited by 114
Metadata
- Authors
- Donner, K., Ollikainen, M., Ridanpää, M., Christen, H.-J., Goebel, H. H., de Visser, M., Pelin, K., & Wallgren-Pettersson, C.
- Venue
- Neuromuscular Disorders
- Publisher
- Elsevier BV
- Published
- 2002-02
- Volume
- 12
- Issue
- 2
- Pages
- 151-158
- ISSN
- 0960-8966 (ISSN-L)
- OpenAlex
- W2092436786
- Cited by
- 227
- References
- 0
- FWCI
- 4.75
- Type
- journal article
- Language
- en
- Open access
- closed
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
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How to cite
Cite CoChat for the checks on this page, and the paper for its own findings.
- This page
- CoChat. (2026). Citation check: Mutations in the β-tropomyosin (TPM2) gene – a rare cause of nemaline myopathy. https://app.cochat.ai/papers/10.1016/s0960-8966(01)00252-8
- The paper
- Donner, K., Ollikainen, M., Ridanpää, M., Christen, H.-J., Goebel, H. H., de Visser, M., Pelin, K., & Wallgren-Pettersson, C. (2002). Mutations in the β-tropomyosin (TPM2) gene – a rare cause of nemaline myopathy. Neuromuscular Disorders. https://doi.org/10.1016/s0960-8966(01)00252-8
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.
