The DOI matches its Crossref record; 1 of the 1 references it cites were found in a registry or an index.
Short GCG expansions in the PABP2 gene cause oculopharyngeal muscular dystrophy
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Scherzinger, E., Lurz, R., Turmaine, M., Mangiarini, L., Hollenbach, B., Hasenbank, R., Bates, G. P., Davies, S. W., Lehrach, H., & Wanker, E. E. (1997) · Cell · doi:10.1016/s0092-8674(00)80514-0 · Cited by 1,291
Cited by
Emery, A. E. (2002) · The Lancet · doi:10.1016/s0140-6736(02)07815-7 · Cited by 1,667
RNA‐binding proteins and post‐transcriptional gene regulation
Glisovic, T., Bachorik, J. L., Yong, J., & Dreyfuss, G. (2008) · FEBS Letters · doi:10.1016/j.febslet.2008.03.004 · Cited by 1,398
30 years of repeat expansion disorders: What have we learned and what are the remaining challenges?
Depienne, C., & Mandel, J.-L. (2021) · The American Journal of Human Genetics · doi:10.1016/j.ajhg.2021.03.011 · Cited by 429
The Poly(A)-Binding Protein Nuclear 1 Suppresses Alternative Cleavage and Polyadenylation Sites
Jenal, M., Elkon, R., Loayza-Puch, F., van Haaften, G., Kühn, U., Menzies, F. M., Vrielink, J. A. F. O., Bos, A. J., Drost, J., Rooijers, K., et al. (2012) · Cell · doi:10.1016/j.cell.2012.03.022 · Cited by 339
The landscape of human STR variation
Willems, T., Gymrek, M., Highnam, G., The 1000 Genomes Project Consortium, Mittelman, D., & Erlich, Y. (2014) · Genome Research · doi:10.1101/gr.177774.114 · Cited by 283
Metadata
- Authors
- Brais, B., Bouchard, J.-P., Xie, Y.-G., Rochefort, D. L., Chrétien, N., Tomé, F. M. S., Lafrentére, R. G., Rommens, J. M., Uyama, E., Nohira, O., Blumen, S., Korcyn, A. D., Heutink, P., Mathieu, J., Duranceau, A., Codère, F., Fardeau, M., & Rouleau, G. A.
- Venue
- Nature Genetics
- Published
- 1998-02-01
- Volume
- 18
- Issue
- 2
- Pages
- 164-167
- ISSN
- 1061-4036 (ISSN-L)
- 1546-1718
- OpenAlex
- W2113559242
- Cited by
- 805
- References
- 1
- FWCI
- 14.35
- Type
- journal article
- Language
- en
- Open access
- green
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- CoChat. (2026). Citation check: Short GCG expansions in the PABP2 gene cause oculopharyngeal muscular dystrophy. https://app.cochat.ai/papers/10.1038/ng0298-164
- The paper
- Brais, B., Bouchard, J.-P., Xie, Y.-G., Rochefort, D. L., Chrétien, N., Tomé, F. M. S., Lafrentére, R. G., Rommens, J. M., Uyama, E., Nohira, O., Blumen, S., Korcyn, A. D., Heutink, P., Mathieu, J., Duranceau, A., Codère, F., Fardeau, M., & Rouleau, G. A. (1998). Short GCG expansions in the PABP2 gene cause oculopharyngeal muscular dystrophy. Nature Genetics. https://doi.org/10.1038/ng0298-164
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.
