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...

पूर्ण विवरण

में बचाया:
ग्रंथसूची विवरण
मुख्य लेखकों: 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
स्वरूप: Artigo
भाषा:Inglês
प्रकाशित: 2007
विषय:
Article
ऑनलाइन पहुंच: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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