Connexin 43 (GJA1) mutations cause the pleiotropic phenotype of oculodentodigital dysplasia

William A. Paznekas, Simeon Boyd, Robert E. Shapiro, Otto Daniels, Bernd Wollnik, Catherine E. Keegan, Jeffrey W. Innis, Mary Beth Dinulos, Cathy Christian, Mark C. Hannibal, Ethylin Wang Jabs

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Medicine & Life Sciences