The DOI matches its Crossref record.
Genotype–phenotype correlation in inherited brain myelination defects due to proteolipid protein gene mutations
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Citations
Cited by
Remyelination in the CNS: from biology to therapy
Franklin, R. J. M., & ffrench-Constant, C. (2008) · Nature Reviews Neuroscience · doi:10.1038/nrn2480 · Cited by 1,544
Myelin in the Central Nervous System: Structure, Function, and Pathology
Stadelmann, C., Timmler, S., Barrantes-Freer, A., & Simons, M. (2019) · Physiological Reviews · doi:10.1152/physrev.00031.2018 · Cited by 728
Hereditary spastic paraplegia: Clinical-genetic characteristics and evolving molecular mechanisms
Lo Giudice, T., Lombardi, F., Santorelli, F. M., Kawarai, T., & Orlacchio, A. (2014) · Experimental Neurology · doi:10.1016/j.expneurol.2014.06.011 · Cited by 347
Inoue, K. (2005) · Neurogenetics · doi:10.1007/s10048-004-0207-y · Cited by 285
Uhlenberg, B., Schuelke, M., Rüschendorf, F., Ruf, N., Kaindl, A. M., Henneke, M., Thiele, H., Stoltenburg-Didinger, G., Aksu, F., Topaloğlu, H., et al. (2004) · The American Journal of Human Genetics · doi:10.1086/422763 · Cited by 271
Metadata
- Authors
- Clinical European Network on Brain Dysmyelinating Disease†, Cailloux, F., Gauthier-Barichard, F., Mimault, C., Isabelle, V., Courtois, V., Giraud, G., Dastugue, B., & Boespflug-Tanguy, O.
- Venue
- European Journal of Human Genetics
- Published
- 2000-10-31
- Volume
- 8
- Issue
- 11
- Pages
- 837-845
- ISSN
- 1018-4813 (ISSN-L)
- 1476-5438
- OpenAlex
- W173955245
- Cited by
- 191
- References
- 0
- FWCI
- 1.59
- 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.
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How to cite
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- This page
- CoChat. (2026). Citation check: Genotype–phenotype correlation in inherited brain myelination defects due to proteolipid protein gene mutations. https://app.cochat.ai/papers/10.1038/sj.ejhg.5200537
- The paper
- Clinical European Network on Brain Dysmyelinating Disease†, Cailloux, F., Gauthier-Barichard, F., Mimault, C., Isabelle, V., Courtois, V., Giraud, G., Dastugue, B., & Boespflug-Tanguy, O. (2000). Genotype–phenotype correlation in inherited brain myelination defects due to proteolipid protein gene mutations. European Journal of Human Genetics. https://doi.org/10.1038/sj.ejhg.5200537
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.
