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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Gorde:
Xehetasun bibliografikoak
Egile Nagusiak: 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
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: 2007
Gaiak:
Article
Sarrera elektronikoa: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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