A deletion mutation along with a novel DNA variation in OCRL cause Lowe syndrome in a child with multiple secondary manifestations
| Autor: | Alireza Paniri, Sadegh Fattahi, Ahmad Rasoulinejad, Haleh Akhavan-Niaki |
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| Jazyk: | angličtina |
| Rok vydání: | 2021 |
| Předmět: | |
| Zdroj: | International Journal of Ophthalmology, Vol 14, Iss 4, Pp 636-638 (2021) |
| Druh dokumentu: | article |
| ISSN: | 2222-3959 2227-4898 |
| DOI: | 10.18240/ijo.2021.04.25 |
| Databáze: | Directory of Open Access Journals |
| Externí odkaz: |
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