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GJA1 mutations, variants, and connexin 43 dysfunction as it relates to the oculodentodigital dysplasia phenotype
? TBD
scientific article published on May 2009
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Scholarly article
Author
Lionel Van Maldergem
Ethylin Wang Jabs
Sascha Vermeer
Martin Delatycki
Pasi A. Koivisto
Joann N Bodurtha
Subject
Phenotype
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