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GJA1 mutations, variants, and connexin 43 dysfunction as it relates to the oculodentodigital dysplasia phenotype
scientific article published on May 2009
Author/s
author: Lionel Van Maldergem, Ethylin Wang Jabs, Sascha Vermeer, Martin Delatycki, Pasi A. Koivisto, Joann N Bodurtha
Work details
Publication date
May 1, 2009
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Language
English
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