Connexin 43 (GJA1) Mutations Cause the Pleiotropic Phenotype of Oculodentodigital Dysplasia.
Paznekas, William A.; Boyadjiev, Simeon A.; Shapiro, Robert E.; Daniels, Otto; Wollnik, Bernd; Keegan, Catherine E.; Innis, Jeffrey W.; Dinulos, Mary Beth; Christian, Cathy; Hannibal, Mark C.; jabs, Ethylin Wang; American Journal of Human Genetics, 2003, vol. 72, issue 2, p 408, ISSN 00029297. ISBN 00029297.

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