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bibliographicCitation Schatz P, Ponjavic V, Andréasson S, McGee TL, Dryja TP, Abrahamson M. Clinical phenotype in a Swedish family with a mutation in the IMPDH1 gene. Ophthalmic Genet. 2005 Sep;26(3):119–24. doi: 10.1080/13816810500229090. PMID: 16272056.
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title Clinical Phenotype in a Swedish Family with a Mutation in theIMPDH1Gene
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