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Claypool SM, Whited K, Srijumnong S, Han X, Koehler CM. Barth syndrome mutations that cause tafazzin complex lability. J Cell Biol. 2011 Feb 7;192(3):447-62. doi: 10.1083/jcb.201008177. © 2011 Claypool et al. This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 3.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/3.0/).
Claypool, Steven M.; Whited, Kevin; Srijumnong, Santi; Han, Xianlin; and Koehler, Carla M., "Barth syndrome mutations that cause tafazzin complex lability." Journal of Cell Biology. 192, 3. 447 - 462. (2011).