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Publication
Novel de novo FOXC1 nonsense mutation in an Axenfeld-Rieger syndrome patient
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Advisor(s)
Abstract(s)
Description
Keywords
Anomalias Congénitas do Olho FOXC1 Protein Human Eye Abnormalities FOXC1 protein, human
Citation
Am J Med Genet A. 2017 Jun;173(6):1607-1610.