The DOI matches its Crossref record; 2 of the 2 references it cites were found in a registry or an index.
Exome Sequencing Reveals Mutations in TRPV3 as a Cause of Olmsted Syndrome
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Citations
Cites
Kumar, P., Henikoff, S., & Ng, P. C. (2009) · Nature Protocols · doi:10.1038/nprot.2009.86 · Cited by 6,521
Rate, molecular spectrum, and consequences of human mutation
Lynch, M. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0912629107 · Cited by 792
Cited by
Advances in TRP channel drug discovery: from target validation to clinical studies
Koivisto, A.-P., Belvisi, M. G., Gaudet, R., & Szallasi, A. (2022) · Nature Reviews Drug Discovery · doi:10.1038/s41573-021-00268-4 · Cited by 537
Transient receptor potential (TRP) channels: a clinical perspective
Kaneko, Y., & Szallasi, A. (2014) · British Journal of Pharmacology · doi:10.1111/bph.12414 · Cited by 370
Akiyama, T., & Carstens, E. (2013) · Neuroscience · doi:10.1016/j.neuroscience.2013.07.035 · Cited by 272
Loss-of-function mutations in HOXC13 cause pure hair and nail ectodermal dysplasia
Lin, Z., Chen, Q., Shi, L., Lee, M., Giehl, K. A., Tang, Z., Wang, H., Zhang, J., Yin, J., Wu, L., et al. (2012) · The American Journal of Human Genetics · doi:10.1016/j.ajhg.2012.08.029 · Cited by 79
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Metadata
- Authors
- Lin, Z., Chen, Q., Lee, M., Cao, X., Zhang, J., Ma, D., Chen, L., Hu, X., Wang, H., Wang, X., Zhang, P., Liu, X., Guan, L., Tang, Y., Yang, H., Tu, P., Bu, D., Zhu, X., Wang, K., Li, R., & Yang, Y.
- Venue
- The American Journal of Human Genetics
- Publisher
- Elsevier BV
- Published
- 2012-03
- Volume
- 90
- Issue
- 3
- Pages
- 558-564
- ISSN
- 0002-9297 (ISSN-L)
- OpenAlex
- W2057154060
- Cited by
- 336
- References
- 2
- FWCI
- 16.65
- Type
- journal article
- Language
- en
- Open access
- bronze
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- The paper
- Lin, Z., Chen, Q., Lee, M., Cao, X., Zhang, J., Ma, D., Chen, L., Hu, X., Wang, H., Wang, X., Zhang, P., Liu, X., Guan, L., Tang, Y., Yang, H., Tu, P., Bu, D., Zhu, X., Wang, K., . . . Yang, Y. (2012). Exome Sequencing Reveals Mutations in TRPV3 as a Cause of Olmsted Syndrome. The American Journal of Human Genetics. https://doi.org/10.1016/j.ajhg.2012.02.006
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.
