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Dive into the research topics of 'An initiator codon mutation in ornithine-δ-aminotransferase causing gyrate atrophy of the choroid and retina'. Together they form a unique fingerprint.- Sort by
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G. A. Mitchell, L. C. Brody, J. Looney, G. Steel, M. Suchanek, C. Dowling, V. Der Kaloustian, M. Kaiser-Kupfer, D. Valle
Research output: Contribution to journal › Article › peer-review