Connexin 43 (GJA1) Mutations Cause the Pleiotropic Phenotype of Oculodentodigital Dysplasia
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- 1 February 2003
- journal article
- research article
- Published by Elsevier in American Journal of Human Genetics
- Vol. 72 (2) , 408-418
- https://doi.org/10.1086/346090
Abstract
No abstract availableKeywords
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