Spectrum and frequency of mutations in IMPDH1 associated with autosomal dominant retinitis pigmentosa and leber congenital amaurosis

Sara J. Bowne, Lori S. Sullivan, Sarah E. Mortimer, Lizbeth Hedstrom, Jingya Zhu, Catherine J. Spellicy, Anisa I. Gire, Dianna Hughbanks-Wheaton, David G. Birch, Richard A. Lewis, John R. Heckenlively, Stephen P. Daiger

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