First report of c.425-1G>A mutation in ornithine...

European Journal of Ophthalmology 2020 / 05

First report of c.425-1G>A mutation in ornithine aminotransferase gene causing gyrate atrophy of the choroid and retina with hyperornithinemia

Jalali, Hossein, Najafi, Mojtaba, Khoshaeen, Atefeh, Mahdavi, Mohammad Reza, Mahdavi, Mahan
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Journal:
European Journal of Ophthalmology
DOI:
10.1177/1120672120921734
Date:
May, 2020
File:
PDF, 199 KB
2020
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