The DOI matches its Crossref record; 3 of the 3 references it cites were found in a registry or an index.
KCNJ2 Mutation Results in Andersen Syndrome with Sex-Specific Cardiac and Skeletal Muscle Phenotypes
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Cites
Hamill, O. P., Marty, A., Neher, E., Sakmann, B., & Sigworth, F. J. (1981) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/bf00656997 · Cited by 18,436
Laitinen, P. J., Brown, K. M., Piippo, K., Swan, H., Devaney, J. M., Brahmbhatt, B., Donarum, E. A., Marino, M., Tiso, N., Viitasalo, M., et al. (2001) · Circulation · doi:10.1161/01.cir.103.4.485 · Cited by 726 · cited 1×
“1 (KCNJ2) have established the genetic heterogeneity of polymorphic ventricular tachycardia (Lahat et al. 2001; Laitinen et al. 2001; Plaster et al. 2001; Priori et al. 2001).”
BackgroundLahat, H., Pras, E., Olender, T., Avidan, N., Ben-Asher, E., Man, O., Levy-Nissenbaum, E., Khoury, A., Lorber, A., Goldman, B., et al. (2001) · The American Journal of Human Genetics · doi:10.1086/324565 · Cited by 655
Cited by
Inwardly Rectifying Potassium Channels: Their Structure, Function, and Physiological Roles
Hibino, H., Inanobe, A., Furutani, K., Murakami, S., Findlay, I., & Kurachi, Y. (2010) · Physiological Reviews · doi:10.1152/physrev.00021.2009 · Cited by 1,539
The primary periodic paralyses: diagnosis, pathogenesis and treatment
Venance, S. L., Cannon, S. C., Fialho, D., Fontaine, B., Hanna, M. G., Ptacek, L. J., Tristani-Firouzi, M., Tawil, R., & Griggs, R. C. (2006) · Brain · doi:10.1093/brain/awh639 · Cited by 370
The QT syndromes: long and short
Morita, H., Wu, J., & Zipes, D. P. (2008) · The Lancet · doi:10.1016/s0140-6736(08)61307-0 · Cited by 317
Long QT syndrome: from channels to cardiac arrhythmias
Moss, A. J. (2005) · Journal of Clinical Investigation · doi:10.1172/jci25537 · Cited by 296
GATA5 loss-of-function mutations associated with congenital bicuspid aortic valve
SHI, L.-M., TAO, J.-W., QIU, X.-B., WANG, J., YUAN, F., XU, L., LIU, H., LI, R.-G., XU, Y.-J., WANG, Q., et al. (2014) · International Journal of Molecular Medicine · doi:10.3892/ijmm.2014.1700 · Cited by 95
Metadata
- Authors
- Andelfinger, G., Tapper, A. R., Welch, R. C., Vanoye, C. G., George, A. L., & Benson, D. W.
- Venue
- The American Journal of Human Genetics
- Publisher
- Elsevier BV
- Published
- 2002-09
- Volume
- 71
- Issue
- 3
- Pages
- 663-668
- ISSN
- 0002-9297 (ISSN-L)
- OpenAlex
- W2017263107
- Cited by
- 262
- References
- 3
- FWCI
- 6.85
- Type
- journal article
- Language
- en
- Open access
- bronze
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- CoChat. (2026). Citation check: KCNJ2 Mutation Results in Andersen Syndrome with Sex-Specific Cardiac and Skeletal Muscle Phenotypes. https://app.cochat.ai/papers/10.1086/342360
- The paper
- Andelfinger, G., Tapper, A. R., Welch, R. C., Vanoye, C. G., George, A. L., & Benson, D. W. (2002). KCNJ2 Mutation Results in Andersen Syndrome with Sex-Specific Cardiac and Skeletal Muscle Phenotypes. The American Journal of Human Genetics. https://doi.org/10.1086/342360
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.
