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- W1999823721 abstract "Significance Wolf–Hirschhorn syndrome (WHS), caused by deletions in 4p16.3, was the first recognized subtelomeric deletion syndrome. As with other syndromes of this class, WHS has not yet been subjected to an intensive, systematic analysis using mouse or cellular models. We recently identified leucine zipper-EF-hand containing transmembrane protein 1 (Letm1) as a mitochondrial Ca 2+ /H + antiporter, located in the core WHS region. In this study, Letm1 null mice were generated and characterized. Deletion of Letm1 disrupts early embryonic development, reduces glucose oxidation and thus particularly affects brain function." @default.
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- W1999823721 date "2013-05-28" @default.
- W1999823721 modified "2023-09-29" @default.
- W1999823721 title "Letm1, the mitochondrial Ca <sup>2+</sup> /H <sup>+</sup> antiporter, is essential for normal glucose metabolism and alters brain function in Wolf–Hirschhorn syndrome" @default.
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- W1999823721 doi "https://doi.org/10.1073/pnas.1308558110" @default.
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