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Dive into the research topics of 'The Gly56Arg mutation in NR2E3 accounts for 1-2% of autosomal dominant retinitis pigmentosa'. Together they form a unique fingerprint.- Sort by
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Anisa I. Gire, Lori S. Sullivan, Sara J. Bowne, David G. Birch, Dianna Hughbanks-Wheaton, John R. Heckenlively, Stephen P. Daiger
Research output: Contribution to journal › Article › peer-review