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SERCA2 Haploinsufficiency in a Mouse Model of Darier Disease Causes a Selective Predisposition to Heart Failure
Null mutations in one copy of ATP2A2, the gene encoding sarco/endoplasmic reticulum Ca(2+)-ATPase isoform 2 (SERCA2), cause Darier disease in humans, a skin condition involving keratinocytes. Cardiac function appears to be unimpaired in Darier disease patients, with no evidence that SERCA2 haploinsu...
Autores principales: | Prasad, Vikram, Lorenz, John N., Lasko, Valerie M., Nieman, Michelle L., Huang, Wei, Wang, Yigang, Wieczorek, David W., Shull, Gary E. |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2015
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4433638/ https://www.ncbi.nlm.nih.gov/pubmed/26064889 http://dx.doi.org/10.1155/2015/251598 |
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