A deletion mutation along with a novel DNA variation in OCRL cause Lowe syndrome in a child with multiple secondary manifestations
oleh: Alireza Paniri, Sadegh Fattahi, Ahmad Rasoulinejad, Haleh Akhavan-Niaki
| Format: | Article |
|---|---|
| Diterbitkan: | Press of International Journal of Ophthalmology (IJO PRESS) 2021-04-01 |
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