The conditional connexin43G138R mouse mutant represents a new model of hereditary oculodentodigital dysplasia in humans

Oculodentodigital dysplasia (ODDD) is a dominant negatively inherited disorder with variable but characteristic anomalies of the fingers and toes, eyes, face and teeth, which are caused by mutations in the connexin 43 (Cx43) gene. All mutations analyzed so far have a negative influence on the conduc...

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Detalhes bibliográficos
Main Authors: Dobrowolski, Radoslaw, Sasse, Philipp, Schrickel, Jan W., Watkins, Marcus, Kim, Jung-Sun, Rackauskas, Mindaugas, Troatz, Clemens, Ghanem, Alexander, Tiemann, Klaus, Degen, Joachim, Bukauskas, Feliksas F., Civitelli, Roberto, Lewalter, Thorsten, Fleischmann, Bernd K., Willecke, Klaus
Formato: Artigo
Idioma:Inglês
Publicado em: 2007
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2847779/
https://ncbi.nlm.nih.gov/pubmed/18003637
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddm329
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