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Frontiers | A Novel Homozygous Variant in GJA1 Causing a Hallermann-Streiff/ Oculodentodigital Dysplasia Overlapping Phenotype: A Clinical Report
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Figure 2 from A novel GJA1 mutation in oculodentodigital dysplasia with progressive spastic paraplegia and sensory deficits. | Semantic Scholar
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