Connexin 43 (GJA1) mutations cause the pleiotropic phenotype of oculodentodigital dysplasia (Q24610890)
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English | Connexin 43 (GJA1) mutations cause the pleiotropic phenotype of oculodentodigital dysplasia |
scientific article |
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Connexin 43 (GJA1) mutations cause the pleiotropic phenotype of oculodentodigital dysplasia (English)
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February 2003
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72
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2
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408-18
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