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Title:	Genome-wide RNAi screen identifies Letm1 as a mitochondrial Ca2+/H+ antiporter
Source:	Science [0036-8075] Jiang, D yr:2009

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description	18.	Letters, E. "Phenotypic integration: studying the ecology and evolution of complex phenotypes." Ecology letters 6.3 (2003): 265-272.
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