The DOI matches its Crossref record.
De-novo mutation in hereditary motor and sensory neuropathy type I
Overview
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Citations
Cited by
Structural Variation in the Human Genome and its Role in Disease
Stankiewicz, P., & Lupski, J. R. (2010) · Annual Review of Medicine · doi:10.1146/annurev-med-100708-204735 · Cited by 1,201
Mutations in ABCC6 cause pseudoxanthoma elasticum
Bergen, A. A. B., Plomp, A. S., Schuurman, E. J., Terry, S., Breuning, M., Dauwerse, H., Swart, J., Kool, M., van Soest, S., Baas, F., et al. (2000) · Nature Genetics · doi:10.1038/76109 · Cited by 593
Self-citationPentao, L., Wise, C. A., Chinault, A. C., Patel, P. I., & Lupski, J. R. (1992) · Nature Genetics · doi:10.1038/ng1292-292 · Cited by 386
Metadata
- Authors
- Hoogendijk, J. E., Hensels, G. W., Janssen, E. A. M., Valentijn, L. J., Baas, F., de Visser, M., Bolhuis, P. A., Gabreels-Festen, A. A. W. M., Gabreels, F. J. M., de onghe, P., Martin, J.-J., & van Broeckhoven, C.
- Venue
- The Lancet
- Publisher
- Elsevier BV
- Published
- 1992-05
- Volume
- 339
- Issue
- 8801
- Pages
- 1081-1082
- ISSN
- 0099-5355 (ISSN-L)
- 0140-6736
- OpenAlex
- W2169412991
- Cited by
- 164
- References
- 0
- FWCI
- 6.99
- 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.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
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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: De-novo mutation in hereditary motor and sensory neuropathy type I. https://app.cochat.ai/papers/10.1016/0140-6736(92)90668-s
- The paper
- Hoogendijk, J. E., Hensels, G. W., Janssen, E. A. M., Valentijn, L. J., Baas, F., de Visser, M., Bolhuis, P. A., Gabreels-Festen, A. A. W. M., Gabreels, F. J. M., de onghe, P., Martin, J.-J., & van Broeckhoven, C. (1992). De-novo mutation in hereditary motor and sensory neuropathy type I. The Lancet. https://doi.org/10.1016/0140-6736(92)90668-s
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.
