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Clinical phenotype in congenital muscular dystrophy: correlation with expression of merosin in skeletal
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Citations
Cited by
Mercuri, E., & Muntoni, F. (2013) · The Lancet · doi:10.1016/s0140-6736(12)61897-2 · Cited by 434
Mutations in the integrin α7 gene cause congenital myopathy
Hayashi, Y. K., Chou, F.-L., Engvall, E., Ogawa, M., Matsuda, C., Hirabayashi, S., Yokochi, K., Ziober, B. L., Kramer, R. H., Kaufman, S. J., et al. (1998) · Nature Genetics · doi:10.1038/ng0598-94 · Cited by 366
The congenital muscular dystrophies in 2004: a century of exciting progress
Muntoni, F., & Voit, T. (2004) · Neuromuscular Disorders · doi:10.1016/j.nmd.2004.06.009 · Cited by 277
Dystrophin in the Nervous System
Lidov, H. G. W. (1996) · Brain Pathology · doi:10.1111/j.1750-3639.1996.tb00783.x · Cited by 110
ADHESION MOLECULES AND INHERITED DISEASES OF THE HUMAN NERVOUS SYSTEM
Kamiguchi, H., Hlavin, M. L., Yamasaki, M., & Lemmon, V. (1998) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.21.1.97 · Cited by 104
Metadata
- Authors
- Philpot, J., Sewry, C., Pennock, J., & Dubowitz, V.
- Venue
- Neuromuscular Disorders
- Publisher
- Elsevier BV
- Published
- 1995-07
- Volume
- 5
- Issue
- 4
- Pages
- 301-305
- ISSN
- 0960-8966 (ISSN-L)
- OpenAlex
- W2052748640
- Cited by
- 182
- References
- 0
- FWCI
- 6.99
- Type
- journal article
- Language
- en
- Open access
- closed
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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: Clinical phenotype in congenital muscular dystrophy: correlation with expression of merosin in skeletal. https://app.cochat.ai/papers/10.1016/0960-8966(94)00069-l
- The paper
- Philpot, J., Sewry, C., Pennock, J., & Dubowitz, V. (1995). Clinical phenotype in congenital muscular dystrophy: correlation with expression of merosin in skeletal. Neuromuscular Disorders. https://doi.org/10.1016/0960-8966(94)00069-l
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.
