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Amedeo Smart
Independent Medical Education
Jalali H, Najafi M, Khoshaeen A, Mahdavi MR, et al. First report of c.425-1G>A mutation in ornithine aminotransferase gene causing gyrate atrophy of the choroid and retina with hyperornithinemia. Eur J Ophthalmol 2021;31:NP23-NP26.PMID: 32418451
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