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Dive into the research topics of 'Unilateral cone-rod dysfunction and retinal thinning in a child carrying the 14484 mutation of Leber hereditary optic neuropathy'. Together they form a unique fingerprint.- Sort by
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Ahmed Kassem, Rustum Karanjia, Collin McClelland, Alfredo Sadun, Michael S. Lee
Research output: Contribution to journal › Article › peer-review