reference/10584192

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/10584192

Outgoing Links

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bibliographicCitation	Dobrowolski R, Sasse P, Schrickel JW, Watkins M, Kim JS, Rackauskas M, Troatz C, Ghanem A, Tiemann K, Degen J, Bukauskas FF, Civitelli R, Lewalter T, Fleischmann BK, Willecke K. 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. PMID: 18003637; PMCID: PMC2847779.
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language	English
source	https://pubmed.ncbi.nlm.nih.gov/ https://www.crossref.org/
title	The conditional connexin43G138R mouse mutant represents a new model of hereditary oculodentodigital dysplasia in humans
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