The DOI matches its Crossref record; 2 of the 2 references it cites were found in a registry or an index.
Mutation of BSND causes Bartter syndrome with sensorineural deafness and kidney failure
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Citations
Cites
Gapped BLAST and PSI-BLAST: a new generation of protein database search programs
Altschul, S. (1997) · Nucleic Acids Research · doi:10.1093/nar/25.17.3389 · Cited by 73,302
The sequence of the human genome
Venter, J. C., Adams, M. D., Myers, E. W., Li, P. W., Mural, R. J., Sutton, G. G., Smith, H. O., Yandell, M., Evans, C. A., Holt, R. A., et al. (2001) · Science · doi:10.1126/science.1058040 · Cited by 13,909
Cited by
Magnesium in man: implications for health and disease
de Baaij, J. H. F., Hoenderop, J. G. J., & Bindels, R. J. M. (2015) · Physiological Reviews · doi:10.1152/physrev.00012.2014 · Cited by 1,726
Molecular Structure and Physiological Function of Chloride Channels
Jentsch, T. J., Stein, V., Weinreich, F., & Zdebik, A. A. (2002) · Physiological Reviews · doi:10.1152/physrev.00029.2001 · Cited by 1,256
Rare independent mutations in renal salt handling genes contribute to blood pressure variation
Ji, W., Foo, J. N., O'Roak, B. J., Zhao, H., Larson, M. G., Simon, D. B., Newton-Cheh, C., State, M. W., Levy, D., & Lifton, R. P. (2008) · Nature Genetics · doi:10.1038/ng.118 · Cited by 812
Salt Sensitivity of Blood Pressure: A Scientific Statement From the American Heart Association
Elijovich, F., Weinberger, M. H., Anderson, C. A. M., Appel, L. J., Bursztyn, M., Cook, N. R., Dart, R. A., Newton-Cheh, C. H., Sacks, F. M., & Laffer, C. L. (2016) · Hypertension · doi:10.1161/hyp.0000000000000047 · Cited by 482
Inherited Disorders of Renal Salt Homeostasis
Scholl, U. I., & Lifton, R. P. (2013) · Seldin and Giebisch's The Kidney · doi:10.1016/b978-0-12-381462-3.00036-7 · Cited by 10
Metadata
- Authors
- Birkenhäger, R., Otto, E., Schürmann, M. J., Vollmer, M., Ruf, E.-M., Maier-Lutz, I., Beekmann, F., Fekete, A., Omran, H., Feldmann, D., Milford, D. V., Jeck, N., Konrad, M., Landau, D., Knoers, N. V. A. M., Antignac, C., Sudbrak, R., Kispert, A., & Hildebrandt, F.
- Venue
- Nature Genetics
- Published
- 2001-10-22
- Volume
- 29
- Issue
- 3
- Pages
- 310-314
- ISSN
- 1061-4036 (ISSN-L)
- 1546-1718
- OpenAlex
- W1608336039
- Cited by
- 539
- References
- 2
- FWCI
- 8.90
- Type
- journal article
- Language
- en
- Open access
- closed
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- This page
- CoChat. (2026). Citation check: Mutation of BSND causes Bartter syndrome with sensorineural deafness and kidney failure. https://app.cochat.ai/papers/10.1038/ng752
- The paper
- Birkenhäger, R., Otto, E., Schürmann, M. J., Vollmer, M., Ruf, E.-M., Maier-Lutz, I., Beekmann, F., Fekete, A., Omran, H., Feldmann, D., Milford, D. V., Jeck, N., Konrad, M., Landau, D., Knoers, N. V. A. M., Antignac, C., Sudbrak, R., Kispert, A., & Hildebrandt, F. (2001). Mutation of BSND causes Bartter syndrome with sensorineural deafness and kidney failure. Nature Genetics. https://doi.org/10.1038/ng752
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.
