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Rhizomelic chondrodysplasia punctata is caused by deficiency of human PEX7, a homologue of the yeast PTS2 receptor
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Citations
Cited by
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Steinberg, S. J., Dodt, G., Raymond, G. V., Braverman, N. E., Moser, A. B., & Moser, H. W. (2006) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2006.09.010 · Cited by 522
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Zhong, T. P., Rosenberg, M., Mohideen, M.-A. P. K., Weinstein, B., & Fishman, M. C. (2000) · Science · doi:10.1126/science.287.5459.1820 · Cited by 422
Purdue, P. E., & Lazarow, P. B. (2001) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev.cellbio.17.1.701 · Cited by 322
Self-citationRefsum disease is caused by mutations in the phytanoyl–CoA hydroxylase gene
Jansen, G. A., Oftnan, R., Ferdinandusse, S., Ijlst, L., Muijsers, A. O., Skjeldal, O. H., Stokke, O., Jakobs, C., Besley, G. T. N., Wraith, J. E., et al. (1997) · Nature Genetics · doi:10.1038/ng1097-190 · Cited by 307
Metadata
- Authors
- Purdue, P. E., Zhang, J. W., Skoneczny, M., & Lazarow, P. B.
- Venue
- Nature Genetics
- Published
- 1997-04
- Volume
- 15
- Issue
- 4
- Pages
- 381-384
- ISSN
- 1061-4036 (ISSN-L)
- 1546-1718
- OpenAlex
- W2073972553
- Cited by
- 265
- References
- 0
- FWCI
- 20.61
- Type
- journal article
- Language
- en
- Open access
- closed
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- CoChat. (2026). Citation check: Rhizomelic chondrodysplasia punctata is caused by deficiency of human PEX7, a homologue of the yeast PTS2 receptor. https://app.cochat.ai/papers/10.1038/ng0497-381
- The paper
- Purdue, P. E., Zhang, J. W., Skoneczny, M., & Lazarow, P. B. (1997). Rhizomelic chondrodysplasia punctata is caused by deficiency of human PEX7, a homologue of the yeast PTS2 receptor. Nature Genetics. https://doi.org/10.1038/ng0497-381
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.