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The conditional connexin43G138R mouse mutant represents a new model of hereditary oculodentodigital dysplasia in humans.
Hum Mol Genet. 2008 Feb 15;17(4):539-54. doi: 10.1093/hmg/ddm329. Epub 2007 Nov 13.
Hum Mol Genet. 2008.
PMID: 18003637
Free PMC article.
Permeability of homotypic and heterotypic gap junction channels formed of cardiac connexins mCx30.2, Cx40, Cx43, and Cx45.
Rackauskas M, Verselis VK, Bukauskas FF.
Rackauskas M, et al.
Am J Physiol Heart Circ Physiol. 2007 Sep;293(3):H1729-36. doi: 10.1152/ajpheart.00234.2007. Epub 2007 Jun 8.
Am J Physiol Heart Circ Physiol. 2007.
PMID: 17557922
Free PMC article.
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